Variant report

Variant	esv1815433
Chromosome Location	chr21:17106192-17167353
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:703)
CpG islands
(count:61)
Chromatin interactive
region (count:68)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:703 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:17133756-17134220	HepG2	liver:	n/a	n/a
2	ARID3A	chr21:17117317-17117631	K562	blood:	n/a	n/a
3	ARID3A	chr21:17113119-17113452	K562	blood:	n/a	n/a
4	ARID3A	chr21:17118246-17118446	K562	blood:	n/a	n/a
5	ARID3A	chr21:17139348-17139571	HepG2	liver:	n/a	n/a
6	ARID3A	chr21:17109712-17109843	K562	blood:	n/a	n/a
7	ARID3A	chr21:17121091-17122489	K562	blood:	n/a	n/a
8	ARID3A	chr21:17116031-17116119	K562	blood:	n/a	n/a
9	ARID3A	chr21:17121292-17121789	HepG2	liver:	n/a	n/a
10	ARID3A	chr21:17107185-17108441	K562	blood:	n/a	n/a
11	ARID3A	chr21:17126991-17127305	HepG2	liver:	n/a	n/a
12	ARID3A	chr21:17110578-17110811	K562	blood:	n/a	n/a
13	ATF1	chr21:17115924-17116267	K562	blood:	n/a	n/a
14	ATF1	chr21:17121788-17121996	K562	blood:	n/a	n/a
15	ATF1	chr21:17114429-17114749	K562	blood:	n/a	n/a
16	ATF2	chr21:17125205-17125852	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr21:17125220-17125829	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr21:17125302-17125720	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr21:17121462-17122162	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr21:17121327-17122205	K562	blood:	n/a	n/a
21	BACH1	chr21:17153194-17153240	K562	blood:	n/a	n/a
22	BACH1	chr21:17146799-17146801	K562	blood:	n/a	n/a
23	BATF	chr21:17106117-17106300	GM12878	blood:	n/a	n/a
24	BATF	chr21:17106178-17106335	GM12878	blood:	n/a	n/a
25	BCL11A	chr21:17125422-17125707	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL11A	chr21:17125425-17125885	H1-hESC	embryonic stem cell:	n/a	n/a
27	BCL11A	chr21:17106121-17106394	GM12878	blood:	n/a	n/a
28	BHLHE40	chr21:17115938-17116086	K562	blood:	n/a	n/a
29	BHLHE40	chr21:17125329-17125681	K562	blood:	n/a	n/a
30	BHLHE40	chr21:17116336-17116344	K562	blood:	n/a	n/a
31	BHLHE40	chr21:17106048-17106420	GM12878	blood:	n/a	n/a
32	CBX3	chr21:17115845-17116273	K562	blood:	n/a	n/a
33	CBX3	chr21:17130646-17130966	K562	blood:	n/a	n/a
34	CCNT2	chr21:17115143-17115381	K562	blood:	n/a	n/a
35	CCNT2	chr21:17114429-17114691	K562	blood:	n/a	n/a
36	CCNT2	chr21:17121825-17122071	K562	blood:	n/a	n/a
37	CEBPB	chr21:17113916-17114327	MCF-7	breast:	n/a	chr21:17114122-17114135 chr21:17114122-17114133 chr21:17114124-17114133 chr21:17114124-17114133 chr21:17114124-17114133 chr21:17114122-17114135 chr21:17114124-17114133 chr21:17114124-17114135 chr21:17114124-17114135 chr21:17114122-17114135
38	CEBPB	chr21:17121407-17121982	K562	blood:	n/a	chr21:17121592-17121605 chr21:17121593-17121604
39	CEBPB	chr21:17121415-17121768	IMR90	lung:	n/a	chr21:17121592-17121605 chr21:17121593-17121604
40	CEBPB	chr21:17113954-17114721	HepG2	liver:	n/a	chr21:17114122-17114135 chr21:17114122-17114133 chr21:17114124-17114133 chr21:17114124-17114133 chr21:17114124-17114133 chr21:17114122-17114135 chr21:17114124-17114133 chr21:17114124-17114135 chr21:17114124-17114135 chr21:17114122-17114135
41	CEBPB	chr21:17148318-17148685	IMR90	lung:	n/a	n/a
42	CEBPB	chr21:17146943-17147230	A549	lung:	n/a	n/a
43	CEBPB	chr21:17121416-17121783	Hela-S3	cervix:	n/a	chr21:17121592-17121605 chr21:17121593-17121604
44	CEBPB	chr21:17108352-17108611	A549	lung:	n/a	n/a
45	CEBPB	chr21:17115682-17115882	HepG2	liver:	n/a	chr21:17115728-17115739
46	CEBPB	chr21:17113970-17114292	Hela-S3	cervix:	n/a	chr21:17114122-17114135 chr21:17114122-17114133 chr21:17114124-17114133 chr21:17114124-17114133 chr21:17114124-17114133 chr21:17114122-17114135 chr21:17114124-17114133 chr21:17114124-17114135 chr21:17114124-17114135 chr21:17114122-17114135
47	CEBPB	chr21:17108387-17108636	K562	blood:	n/a	n/a
48	CEBPB	chr21:17121410-17121763	HepG2	liver:	n/a	chr21:17121592-17121605 chr21:17121593-17121604
49	CEBPB	chr21:17161441-17161794	MCF-7	breast:	n/a	chr21:17161591-17161604
50	CEBPB	chr21:17117410-17117692	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:17106209-17106259	MCF-7	breast:	n/a
2	chr21:17106209-17106259	ECC-1	luminal epithelium:	n/a
3	chr21:17106209-17106259	T-47D	breast:	n/a
4	chr21:17106209-17106259	NHDF-neo	bronchial:	n/a
5	chr21:17106209-17106259	PANC-1	pancreas:	n/a
6	chr21:17106209-17106259	Hepatocyte	liver:	n/a
7	chr21:17106209-17106259	AG10803	skin:	n/a
8	chr21:17106209-17106259	NH-A	brain:	n/a
9	chr21:17106209-17106259	HepG2	liver:	n/a
10	chr21:17106209-17106259	AG09319	gingival:	n/a
11	chr21:17106209-17106259	SK-N-MC	brain:	n/a
12	chr21:17106209-17106259	H1-hESC	embryonic stem cell:	embryo
13	chr21:17106209-17106259	GM19239	blood:	n/a
14	chr21:17106209-17106259	LNCaP	prostate:	n/a
15	chr21:17106209-17106259	NHBE	bronchial:	n/a
16	chr21:17106209-17106259	HCM	heart:	n/a
17	chr21:17106209-17106259	BJ	skin:	n/a
18	chr21:17106209-17106259	HCPEpiC	choroid plexus:	n/a
19	chr21:17106209-17106259	SKMC	muscle:	n/a
20	chr21:17106209-17106259	ProgFib	skin:	n/a
21	chr21:17106209-17106259	HRCEpiC	kidney:	n/a
22	chr21:17106209-17106259	U87	brain:	n/a
23	chr21:17106209-17106259	SAEC	small airway:	n/a
24	chr21:17106209-17106259	Caco-2	colon:	n/a
25	chr21:17106209-17106259	HL-60	blood:	n/a
26	chr21:17106209-17106259	PrEC	prostate:	n/a
27	chr21:17106209-17106259	RPTEC	kidney:	n/a
28	chr21:17106209-17106259	MCF10A-Er-Src	breast:	n/a
29	chr21:17106209-17106259	NT2-D1	testis:	n/a
30	chr21:17106209-17106259	HCT-116	colon:	n/a
31	chr21:17106209-17106259	GM06990	blood:	n/a
32	chr21:17106209-17106259	SK-N-SH_RA	brain:	n/a
33	chr21:17106209-17106259	HEK293	kidney:	embryo
34	chr21:17106209-17106259	HNPCEpiC	eye:	n/a
35	chr21:17106209-17106259	HPAEpiC	pulmonary alveolar:	n/a
36	chr21:17106209-17106259	GM12891	blood:	n/a
37	chr21:17106209-17106259	GM12878	blood:	n/a
38	chr21:17106209-17106259	AG04450	lung:	fetal
39	chr21:17106209-17106259	HMEC	breast:	n/a
40	chr21:17106209-17106259	AG09309	skin:	n/a
41	chr21:17106209-17106259	HRE	kidney:	n/a
42	chr21:17106209-17106259	K562	blood:	n/a
43	chr21:17106209-17106259	ovcar-3	ovarian:	n/a
44	chr21:17106209-17106259	Jurkat	blood:	n/a
45	chr21:17106209-17106259	HIPEpiC	eye:	n/a
46	chr21:17106209-17106259	A549	lung:	n/a
47	chr21:17106209-17106259	AG04449	skin:	fetal
48	chr21:17106209-17106259	Hela-S3	cervix:	n/a
49	chr21:17106209-17106259	IMR90	lung:	fetal
50	chr21:17106209-17106259	BE2_C	brain:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:17144944..17148099-chr21:17149634..17151745,3	K562	blood:
2	chr21:17121263..17123662-chr21:17127297..17128832,2	K562	blood:
3	chr21:17149058..17152250-chr21:17172781..17176398,3	K562	blood:
4	chr21:17101644..17104508-chr21:17160279..17163152,3	K562	blood:
5	chr21:17118340..17121294-chr21:17222829..17224563,2	MCF-7	breast:
6	chr21:17114779..17116844-chr21:17137074..17138622,2	K562	blood:
7	chr21:17126721..17128269-chr21:17130491..17133281,2	MCF-7	breast:
8	chr21:17131546..17134772-chr21:17136356..17138734,3	MCF-7	breast:
9	chr21:17116180..17118994-chr21:17126178..17127711,2	K562	blood:
10	chr21:17102586..17104212-chr21:17132608..17135141,2	K562	blood:
11	chr21:17131546..17134772-chr21:17136356..17138734,3	MCF-7	breast:
12	chr21:17102017..17104012-chr21:17109243..17111259,3	MCF-7	breast:
13	chr21:17141227..17143444-chr21:17164471..17166670,2	K562	blood:
14	chr21:17135749..17138458-chr21:17138787..17142045,4	K562	blood:
15	chr21:17101583..17104455-chr21:17117901..17120462,3	MCF-7	breast:
16	chr21:17135749..17138458-chr21:17138787..17141062,2	K562	blood:
17	chr21:17125584..17127953-chr21:17130378..17132537,2	K562	blood:
18	chr21:17125329..17127564-chr21:17142354..17143881,2	K562	blood:
19	chr21:17100962..17103706-chr21:17140698..17142890,2	MCF-7	breast:
20	chr21:17136575..17138278-chr21:17138392..17140669,2	MCF-7	breast:
21	chr21:17104177..17106318-chr21:17123933..17125566,2	K562	blood:
22	chr21:17125584..17127953-chr21:17130378..17132537,2	K562	blood:
23	chr21:17104089..17106756-chr21:17109896..17112248,2	MCF-7	breast:
24	chr21:17104741..17106433-chr21:17217279..17219157,2	K562	blood:
25	chr21:17141263..17145457-chr21:17148743..17151657,3	MCF-7	breast:
26	chr21:17101984..17103858-chr21:17138166..17141099,3	K562	blood:
27	chr21:17104089..17106756-chr21:17109896..17112248,2	MCF-7	breast:
28	chr21:17150245..17152126-chr21:17152433..17154723,2	MCF-7	breast:
29	chr21:17077309..17079464-chr21:17110319..17112790,2	K562	blood:
30	chr21:17135749..17138458-chr21:17138787..17142045,4	K562	blood:
31	chr21:17127290..17130073-chr21:17133451..17135040,2	MCF-7	breast:
32	chr21:17108742..17111248-chr21:17133909..17136883,3	K562	blood:
33	chr21:17105614..17107368-chr21:17115723..17117449,2	MCF-7	breast:
34	chr21:17105250..17107735-chr21:17192810..17196080,3	K562	blood:
35	chr21:17110916..17112598-chr21:17143499..17145312,2	K562	blood:
36	chr21:17102136..17104047-chr21:17126942..17128676,2	K562	blood:
37	chr21:17128179..17129872-chr21:17129945..17132364,2	K562	blood:
38	chr21:17104587..17106311-chr21:17139989..17141909,2	K562	blood:
39	chr21:17102202..17104266-chr21:17147089..17149632,2	K562	blood:
40	chr21:17104587..17106311-chr21:17139989..17141909,2	K562	blood:
41	chr21:17110916..17112598-chr21:17143499..17145312,2	K562	blood:
42	chr21:17108742..17111248-chr21:17133909..17136883,3	K562	blood:
43	chr21:17136575..17138278-chr21:17138392..17140669,2	MCF-7	breast:
44	chr21:17125329..17127564-chr21:17142354..17143881,2	K562	blood:
45	chr21:17141227..17143444-chr21:17164471..17166670,2	K562	blood:
46	chr21:17139183..17140756-chr21:17159660..17161320,2	K562	blood:
47	chr21:17127290..17130073-chr21:17133451..17135040,2	MCF-7	breast:
48	chr21:17161716..17165746-chr21:17170595..17173686,4	K562	blood:
49	chr21:17123698..17126562-chr21:17142609..17145221,2	MCF-7	breast:
50	chr21:17103751..17105716-chr21:17107281..17109325,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRIP1-11	chr21:17157066-17157167	NONHSAT081214
2	lnc-NRIP1-10	chr21:17117211-17117399	NONHSAT081212
3	lnc-NRIP1-9	chr21:17109812-17109878	NONHSAT081208
4	lnc-NRIP1-11	chr21:17160773-17160867	NONHSAT081214
5	lnc-NRIP1-11	chr21:17159893-17160023	NONHSAT081214
6	lnc-NRIP1-10	chr21:17116323-17116635	NONHSAT081212

No data

Variant related genes	Relation type
USP25	TF binding region
RBPMSLP	TF binding region
USP25	CpG island
RBPMSLP	CpG island
ENSG00000234159	chromatin interactions
ENSG00000155313	chromatin interactions

Extended variants
information (count: 2330 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2330 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188627257	chr21:17106206-17106207	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs557921450	chr21:17106240-17106241	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs370847535	chr21:17106245-17106246	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs545802995	chr21:17106252-17106253	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs559288177	chr21:17106268-17106269	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs528780827	chr21:17106283-17106284	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs926612	chr21:17106310-17106311	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs367884487	chr21:17106374-17106375	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs531051214	chr21:17106389-17106390	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs71317622	chr21:17106396-17106397	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs144069686	chr21:17106419-17106420	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs570563008	chr21:17106436-17106437	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs539497169	chr21:17106478-17106479	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs71317623	chr21:17106504-17106505	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs146604819	chr21:17106544-17106545	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs566504460	chr21:17106550-17106551	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs535417126	chr21:17106576-17106577	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs79763812	chr21:17106595-17106596	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs115961922	chr21:17106602-17106603	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs376183989	chr21:17106639-17106640	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs537641268	chr21:17106733-17106734	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs192695000	chr21:17106748-17106749	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529643651	chr21:17106844-17106845	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs576941716	chr21:17106860-17106861	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs2823464	chr21:17106887-17106888	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs9979887	chr21:17106932-17106933	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs372401975	chr21:17106935-17106936	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs145022541	chr21:17106963-17106964	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs528500454	chr21:17107002-17107003	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs563112119	chr21:17107017-17107018	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs542196886	chr21:17107059-17107060	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs201859610	chr21:17107107-17107108	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs8128012	chr21:17107174-17107175	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs531187316	chr21:17107192-17107193	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs76165251	chr21:17107208-17107209	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs141062780	chr21:17107215-17107216	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs376990748	chr21:17107218-17107219	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553057401	chr21:17107238-17107239	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs28372331	chr21:17107266-17107267	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs566565058	chr21:17107286-17107287	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs8127158	chr21:17107288-17107289	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs150265735	chr21:17107291-17107292	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs371851233	chr21:17107342-17107343	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs569067171	chr21:17107344-17107345	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs145877063	chr21:17107364-17107365	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs566898379	chr21:17107375-17107376	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs73355473	chr21:17107469-17107470	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs549768531	chr21:17107554-17107555	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs148918308	chr21:17107570-17107571	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs184548037	chr21:17107614-17107615	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
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 myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell lymphomas	19863542	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
Acute lymphoblastic leukemia	21980252	CNVD
Metanephric adenoma	20802469	CNVD
Neuroblastoma	18923191	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute myeloid leukemia	21251322	CNVD
abnormal development	18461090	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	18923514	CNVD
Alzheimer''s disease	20877625	CNVD
Follicular lymphoma	20505157	CNVD
Alzheimer''s disease	21956041	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Invasive pancreatic ductal carcinoma	16982739	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
Epilepsy	20502679	CNVD
22q11.2 microdeletion syndrome	19750312	CNVD
Breast cancer	20409316	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2387 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17103200-17114400	Weak transcription	Spleen	Spleen
2	chr21:17103400-17114400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr21:17103600-17106200	Flanking Active TSS	Dnd41	blood
4	chr21:17103800-17106400	Enhancers	Primary B cells from peripheral blood	blood
5	chr21:17103800-17106600	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
6	chr21:17103800-17108400	Weak transcription	Pancreas	Pancrea
7	chr21:17103800-17114400	Weak transcription	Lung	lung
8	chr21:17103800-17115000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr21:17104000-17107200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr21:17104000-17114600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr21:17104000-17114600	Weak transcription	Fetal Muscle Trunk	muscle
12	chr21:17104200-17110800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr21:17104200-17133400	Weak transcription	Colonic Mucosa	Colon
14	chr21:17104600-17111800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr21:17104600-17113000	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr21:17104600-17114600	Weak transcription	Brain Cingulate Gyrus	brain
17	chr21:17104600-17123400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr21:17104800-17106400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr21:17104800-17106400	Weak transcription	Colon Smooth Muscle	Colon
20	chr21:17104800-17111400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr21:17104800-17115000	Weak transcription	Fetal Muscle Leg	muscle
22	chr21:17105000-17106200	Enhancers	Left Ventricle	heart
23	chr21:17105000-17107000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
24	chr21:17105000-17107800	Weak transcription	Ovary	ovary
25	chr21:17105000-17109400	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr21:17105000-17114000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr21:17105200-17106400	Enhancers	Fetal Brain Male	brain
28	chr21:17105400-17106200	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr21:17105400-17106200	Enhancers	Fetal Thymus	thymus
30	chr21:17105400-17106400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr21:17105400-17106400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr21:17105400-17106400	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr21:17105400-17106400	Weak transcription	Adipose Nuclei	Adipose
34	chr21:17105400-17106400	Enhancers	Hela-S3	cervix
35	chr21:17105400-17106400	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr21:17105400-17106600	Enhancers	Primary hematopoietic stem cells	blood
37	chr21:17105400-17106600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr21:17105400-17106600	Enhancers	Liver	Liver
39	chr21:17105400-17106600	Active TSS	Rectal Mucosa Donor 29	rectum
40	chr21:17105400-17106600	Enhancers	HepG2	liver
41	chr21:17105400-17106600	Enhancers	NHEK	skin
42	chr21:17105400-17107000	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr21:17105400-17107200	Weak transcription	Fetal Heart	heart
44	chr21:17105400-17107200	Weak transcription	Fetal Intestine Small	intestine
45	chr21:17105400-17107600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr21:17105400-17107600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr21:17105400-17107600	Weak transcription	Duodenum Mucosa	Duodenum
48	chr21:17105400-17107600	Weak transcription	Osteobl	bone
49	chr21:17105400-17107800	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr21:17105400-17107800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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