Variant report

Variant	esv3431505
Chromosome Location	chr21:45757974-45759872
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:789)
CpG islands
(count:549)
Chromatin interactive
region (count:24)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:789 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:45758316-45758502	HepG2	liver:	n/a	n/a
2	ARID3A	chr21:45759286-45759769	HepG2	liver:	n/a	n/a
3	ATF1	chr21:45759028-45759926	K562	blood:	n/a	n/a
4	ATF2	chr21:45759171-45759646	GM12878	blood:	n/a	n/a
5	ATF2	chr21:45759170-45759501	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr21:45759160-45759460	GM12878	blood:	n/a	n/a
7	ATF3	chr21:45759128-45759498	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr21:45759195-45759483	K562	blood:	n/a	n/a
9	ATF3	chr21:45759035-45759503	HepG2	liver:	n/a	n/a
10	ATF3	chr21:45759140-45759494	HepG2	liver:	n/a	n/a
11	ATF3	chr21:45759036-45759520	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr21:45759099-45759539	K562	blood:	n/a	n/a
13	ATF3	chr21:45759062-45759567	GM12878	blood:	n/a	n/a
14	ATF3	chr21:45758984-45759561	K562	blood:	n/a	n/a
15	BCLAF1	chr21:45759170-45759514	GM12878	blood:	n/a	n/a
16	BHLHE40	chr21:45758981-45759547	K562	blood:	n/a	chr21:45759358-45759374
17	BHLHE40	chr21:45758218-45758468	K562	blood:	n/a	n/a
18	BHLHE40	chr21:45758987-45759519	HepG2	liver:	n/a	chr21:45759358-45759374
19	BHLHE40	chr21:45759039-45759465	GM12878	blood:	n/a	chr21:45759358-45759374
20	BHLHE40	chr21:45758351-45758404	GM12878	blood:	n/a	n/a
21	BRCA1	chr21:45759158-45759408	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr21:45758345-45758408	GM12878	blood:	n/a	n/a
23	BRCA1	chr21:45759069-45759581	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr21:45758362-45758468	HepG2	liver:	n/a	n/a
25	BRCA1	chr21:45759171-45759438	GM12878	blood:	n/a	n/a
26	BRCA1	chr21:45759181-45759470	HepG2	liver:	n/a	n/a
27	CBX3	chr21:45759110-45759618	K562	blood:	n/a	n/a
28	CCNT2	chr21:45758836-45759561	K562	blood:	n/a	chr21:45759158-45759167
29	CEBPB	chr21:45759045-45759411	Hela-S3	cervix:	n/a	n/a
30	CEBPD	chr21:45759110-45759659	K562	blood:	n/a	n/a
31	CEBPD	chr21:45758886-45759529	HepG2	liver:	n/a	n/a
32	CHD1	chr21:45759039-45759771	GM12878	blood:	n/a	n/a
33	CHD1	chr21:45757748-45758570	IMR90	lung:	n/a	n/a
34	CHD1	chr21:45759387-45759612	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr21:45758991-45759880	K562	blood:	n/a	n/a
36	CHD2	chr21:45758425-45758488	K562	blood:	n/a	n/a
37	CHD2	chr21:45759062-45759480	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr21:45758964-45759679	GM12878	blood:	n/a	n/a
39	CHD2	chr21:45757907-45758489	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr21:45759017-45759439	HepG2	liver:	n/a	n/a
41	CHD2	chr21:45758286-45759660	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr21:45758260-45758584	HepG2	liver:	n/a	n/a
43	CHD2	chr21:45758379-45758502	GM12878	blood:	n/a	n/a
44	CREB1	chr21:45758956-45759483	A549	lung:	n/a	n/a
45	CREB1	chr21:45758907-45760034	GM12878	blood:	n/a	n/a
46	CREB1	chr21:45758893-45759659	ECC-1	luminal epithelium:	n/a	n/a
47	CREB1	chr21:45758935-45759832	K562	blood:	n/a	n/a
48	CREB1	chr21:45758842-45759638	A549	lung:	n/a	n/a
49	CREB1	chr21:45758871-45759738	HepG2	liver:	n/a	n/a
50	CREB1	chr21:45758927-45759817	GM12878	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45759020-45759070	ECC-1	luminal epithelium:	n/a
2	chr21:45759502-45759552	PANC-1	pancreas:	n/a
3	chr21:45759228-45759278	HRCEpiC	kidney:	n/a
4	chr21:45759020-45759070	HCM	heart:	n/a
5	chr21:45759733-45759783	GM06990	blood:	n/a
6	chr21:45759016-45759066	SKMC	muscle:	n/a
7	chr21:45759431-45759481	HRE	kidney:	n/a
8	chr21:45758130-45758180	GM12878	blood:	n/a
9	chr21:45759016-45759066	A549	lung:	n/a
10	chr21:45759733-45759783	Caco-2	colon:	n/a
11	chr21:45758130-45758180	Jurkat	blood:	n/a
12	chr21:45759016-45759066	PrEC	prostate:	n/a
13	chr21:45759431-45759481	HCM	heart:	n/a
14	chr21:45759431-45759481	HCT-116	colon:	n/a
15	chr21:45758130-45758180	HNPCEpiC	eye:	n/a
16	chr21:45759733-45759783	HUVEC	blood vessel:	n/a
17	chr21:45759228-45759278	H1-hESC	embryonic stem cell:	embryo
18	chr21:45759431-45759481	MCF-7	breast:	n/a
19	chr21:45758130-45758180	HPAEpiC	pulmonary alveolar:	n/a
20	chr21:45759733-45759783	Hela-S3	cervix:	n/a
21	chr21:45758982-45759032	SKMC	muscle:	n/a
22	chr21:45759733-45759783	HAEpiC	amniotic membrane:	n/a
23	chr21:45759228-45759278	MCF10A-Er-Src	breast:	n/a
24	chr21:45759228-45759278	ovcar-3	ovarian:	n/a
25	chr21:45759502-45759552	GM19239	blood:	n/a
26	chr21:45758982-45759032	MCF10A-Er-Src	breast:	n/a
27	chr21:45759228-45759278	Caco-2	colon:	n/a
28	chr21:45759431-45759481	Caco-2	colon:	n/a
29	chr21:45758982-45759032	GM12878	blood:	n/a
30	chr21:45758130-45758180	HL-60	blood:	n/a
31	chr21:45759439-45759489	GM12892	blood:	n/a
32	chr21:45759228-45759278	Jurkat	blood:	n/a
33	chr21:45758130-45758180	H1-hESC	embryonic stem cell:	embryo
34	chr21:45759439-45759489	ProgFib	skin:	n/a
35	chr21:45759020-45759070	U87	brain:	n/a
36	chr21:45758130-45758180	NHBE	bronchial:	n/a
37	chr21:45759733-45759783	Jurkat	blood:	n/a
38	chr21:45758130-45758180	AG09319	gingival:	n/a
39	chr21:45759016-45759066	K562	blood:	n/a
40	chr21:45758130-45758180	AG04450	lung:	fetal
41	chr21:45759228-45759278	GM12892	blood:	n/a
42	chr21:45758982-45759032	LNCaP	prostate:	n/a
43	chr21:45759733-45759783	SKMC	muscle:	n/a
44	chr21:45759502-45759552	LNCaP	prostate:	n/a
45	chr21:45759502-45759552	ECC-1	luminal epithelium:	n/a
46	chr21:45758982-45759032	GM06990	blood:	n/a
47	chr21:45759439-45759489	PFSK-1	brain:	n/a
48	chr21:45759502-45759552	NH-A	brain:	n/a
49	chr21:45758130-45758180	GM19239	blood:	n/a
50	chr21:45759228-45759278	HAEpiC	amniotic membrane:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45758998..45760559-chr21:45788952..45791849,2	K562	blood:
2	chr21:45758503..45759276-chr5:33440044..33440944,2	Hela-S3	cervix:
3	chr21:45757587..45760440-chr21:45787714..45792009,6	MCF-7	breast:
4	chr21:45758776..45759711-chr5:43483543..43484104,2	Hela-S3	cervix:
5	chr21:45534290..45536622-chr21:45758168..45760821,2	MCF-7	breast:
6	chr21:45572051..45574951-chr21:45759360..45761487,2	MCF-7	breast:
7	chr10:102295304..102296047-chr21:45758837..45759535,2	Hela-S3	cervix:
8	chr21:45757779..45764116-chr21:45768144..45773804,8	K562	blood:
9	chr21:45758316..45760568-chr21:45903461..45906076,2	MCF-7	breast:
10	chr21:45552120..45555319-chr21:45756917..45761085,4	MCF-7	breast:
11	chr21:45756335..45760049-chr21:45874026..45878349,7	MCF-7	breast:
12	chr21:45525933..45529754-chr21:45756924..45759975,4	MCF-7	breast:
13	chr21:45759510..45761170-chr21:45775846..45778122,2	MCF-7	breast:
14	chr21:45758282..45760774-chr21:46492663..46495375,2	K562	blood:
15	chr21:45553374..45555215-chr21:45757736..45759429,2	K562	blood:
16	chr21:45759454..45761302-chr21:45817481..45820269,2	MCF-7	breast:
17	chr21:45759073..45759711-chr6:26157874..26158375,2	Hela-S3	cervix:
18	chr21:45525373..45527219-chr21:45757637..45759650,2	K562	blood:
19	chr21:45759332..45762202-chr21:46401105..46402631,2	K562	blood:
20	chr21:45137459..45139006-chr21:45757903..45760574,2	K562	blood:
21	chr21:45758851..45761192-chr21:45902340..45905536,3	K562	blood:
22	chr21:45719852..45723806-chr21:45756512..45759776,5	MCF-7	breast:
23	chr21:45759142..45761625-chr21:45788983..45791784,2	MCF-7	breast:
24	chr21:45759032..45759920-chr4:76598161..76598715,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRPM2-1	chr21:45759259-45759353	ENSG00000232969.1

No data

Variant related genes	Relation type
ENSG00000232969	TF binding region
C21orf2	TF binding region
ENSG00000232969	CpG island
C21orf2	CpG island
ENSG00000138757	chromatin interactions
ENSG00000260256	chromatin interactions
ENSG00000113407	chromatin interactions
ENSG00000249572	chromatin interactions
ENSG00000166135	chromatin interactions
ENSG00000197381	chromatin interactions
ENSG00000249492	chromatin interactions
ENSG00000141959	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000160233	chromatin interactions
ENSG00000235374	chromatin interactions
ENSG00000142185	chromatin interactions
ENSG00000241945	chromatin interactions
ENSG00000151881	chromatin interactions
ENSG00000228709	chromatin interactions
ENSG00000160209	chromatin interactions
ENSG00000268856	chromatin interactions
ENSG00000229356	chromatin interactions
ENSG00000160221	chromatin interactions

Extended variants
information (count: 79 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:79 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115007048	chr21:45758043-45758044	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
2	rs531007110	chr21:45758044-45758045	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
3	rs550016453	chr21:45758049-45758050	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs561826842	chr21:45758089-45758090	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
5	rs529208649	chr21:45758104-45758105	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs547713142	chr21:45758116-45758117	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs376509584	chr21:45758124-45758125	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs565722595	chr21:45758127-45758128	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs539049448	chr21:45758132-45758133	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs371672911	chr21:45758140-45758141	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs147594889	chr21:45758155-45758156	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs534009281	chr21:45758190-45758191	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs368827073	chr21:45758218-45758219	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs73231264	chr21:45758231-45758232	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs537113160	chr21:45758333-45758334	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
16	rs188852613	chr21:45758341-45758342	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
17	rs181692122	chr21:45758342-45758343	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
18	rs375265632	chr21:45758347-45758348	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
19	rs535030287	chr21:45758392-45758393	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
20	rs553241880	chr21:45758416-45758417	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
21	rs577995881	chr21:45758460-45758461	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
22	rs114140671	chr21:45758463-45758464	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs376503653	chr21:45758502-45758503	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
24	rs114583726	chr21:45758518-45758519	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
25	rs66904159	chr21:45758546-45758547	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
26	rs575660019	chr21:45758554-45758555	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
27	rs543098757	chr21:45758575-45758576	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
28	rs527366002	chr21:45758617-45758618	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
29	rs375273189	chr21:45758618-45758619	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
30	rs111119177	chr21:45758633-45758634	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
31	rs529091604	chr21:45758653-45758654	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
32	rs550556443	chr21:45758663-45758664	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
33	rs547751923	chr21:45758795-45758796	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
34	rs559366777	chr21:45758796-45758797	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
35	rs533224231	chr21:45758839-45758840	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
36	rs551102398	chr21:45758840-45758841	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
37	rs569592565	chr21:45758861-45758862	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
38	rs530522045	chr21:45758877-45758878	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
39	rs189162062	chr21:45758909-45758910	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	mRNA abundance
40	rs567559896	chr21:45758911-45758912	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
41	rs555860989	chr21:45758930-45758931	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
42	rs534873647	chr21:45758944-45758945	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
43	rs182132626	chr21:45758954-45758955	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
44	rs571862837	chr21:45758962-45758963	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
45	rs185961242	chr21:45758966-45758967	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
46	rs557082104	chr21:45759012-45759013	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
47	rs11870	chr21:45759045-45759046	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	20 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs372118549	chr21:45759052-45759053	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
49	rs200351746	chr21:45759053-45759054	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
50	rs375087550	chr21:45759060-45759061	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Williams-beuren syndrome	16826523	CNVD

Chromatin state (count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45725000-45758000	Weak transcription	Right Atrium	heart
2	chr21:45731400-45758000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr21:45731400-45758000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr21:45731400-45758000	Weak transcription	A549	lung
5	chr21:45731600-45758000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr21:45731800-45758000	Weak transcription	HSMM	muscle
7	chr21:45733400-45758000	Weak transcription	Psoas Muscle	Psoas
8	chr21:45734000-45758000	Weak transcription	HUVEC	blood vessel
9	chr21:45734400-45758000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr21:45740200-45758000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr21:45743000-45759000	Weak transcription	Primary B cells from cord blood	blood
12	chr21:45745400-45759000	Weak transcription	Small Intestine	intestine
13	chr21:45745800-45758200	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr21:45746400-45758000	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr21:45746600-45758200	Weak transcription	Primary hematopoietic stem cells	blood
16	chr21:45747600-45758200	Weak transcription	Aorta	Aorta
17	chr21:45747800-45758000	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr21:45748000-45758200	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr21:45750600-45758000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr21:45754400-45758000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr21:45754400-45758000	Weak transcription	NHEK	skin
22	chr21:45755800-45758200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr21:45755800-45758200	Weak transcription	Esophagus	oesophagus
24	chr21:45755800-45758200	Weak transcription	Gastric	stomach
25	chr21:45756400-45758000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr21:45756400-45758000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr21:45756600-45758000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr21:45756600-45758000	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr21:45756600-45758000	Weak transcription	Brain Germinal Matrix	brain
30	chr21:45756600-45758000	Weak transcription	Pancreas	Pancrea
31	chr21:45756600-45758200	Weak transcription	Ovary	ovary
32	chr21:45756600-45758200	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr21:45756600-45758200	Weak transcription	Right Ventricle	heart
34	chr21:45756800-45758000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr21:45756800-45758000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr21:45756800-45758000	Weak transcription	Duodenum Mucosa	Duodenum
37	chr21:45756800-45758000	Weak transcription	Osteobl	bone
38	chr21:45756800-45758200	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr21:45756800-45758200	Weak transcription	Spleen	Spleen
40	chr21:45756800-45758200	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr21:45756800-45759000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr21:45757000-45758000	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr21:45757200-45758000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr21:45757200-45758000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr21:45757200-45758000	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr21:45757200-45758000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr21:45757200-45758000	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr21:45757200-45758000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr21:45757200-45758000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr21:45757200-45758000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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