Variant report

Variant	nsv873213
Chromosome Location	chr1:223885843-223924236
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3015)
CpG islands
(count:1712)
Chromatin interactive
region (count:137)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3015 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:223888558-223889044	K562	blood:	n/a	n/a
2	ARID3A	chr1:223900023-223900206	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:223894300-223894382	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:223914177-223914601	K562	blood:	n/a	n/a
5	ARID3A	chr1:223899721-223900339	K562	blood:	n/a	n/a
6	ARID3A	chr1:223894290-223894501	K562	blood:	n/a	n/a
7	ARID3A	chr1:223885930-223886216	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:223885939-223886268	K562	blood:	n/a	n/a
9	ARID3A	chr1:223895704-223896034	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:223897421-223897635	K562	blood:	n/a	n/a
11	ARID3A	chr1:223902808-223903334	K562	blood:	n/a	n/a
12	ARID3A	chr1:223898262-223898496	K562	blood:	n/a	n/a
13	ATF1	chr1:223914251-223914758	K562	blood:	n/a	n/a
14	ATF1	chr1:223894958-223895653	K562	blood:	n/a	n/a
15	ATF1	chr1:223898256-223898439	K562	blood:	n/a	n/a
16	ATF1	chr1:223902580-223903595	K562	blood:	n/a	n/a
17	ATF2	chr1:223906513-223907022	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr1:223914307-223914800	GM12878	blood:	n/a	n/a
19	ATF2	chr1:223885883-223886313	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr1:223885864-223886288	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr1:223906618-223906992	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr1:223914249-223914814	GM12878	blood:	n/a	n/a
23	ATF3	chr1:223888414-223889418	A549	lung:	n/a	n/a
24	ATF3	chr1:223894675-223895471	A549	lung:	n/a	n/a
25	ATF3	chr1:223888604-223888952	K562	blood:	n/a	n/a
26	ATF3	chr1:223894808-223895281	K562	blood:	n/a	n/a
27	ATF3	chr1:223908547-223909129	A549	lung:	n/a	n/a
28	ATF3	chr1:223914212-223914846	A549	lung:	n/a	n/a
29	ATF3	chr1:223914172-223914713	K562	blood:	n/a	n/a
30	ATF3	chr1:223893758-223894541	A549	lung:	n/a	n/a
31	ATF3	chr1:223899947-223900362	K562	blood:	n/a	chr1:223900268-223900277
32	ATF3	chr1:223908486-223909120	A549	lung:	n/a	n/a
33	ATF3	chr1:223914116-223914867	A549	lung:	n/a	n/a
34	ATF3	chr1:223894948-223895200	K562	blood:	n/a	n/a
35	ATF3	chr1:223899542-223900397	K562	blood:	n/a	chr1:223900268-223900277
36	ATF3	chr1:223894713-223895551	A549	lung:	n/a	n/a
37	ATF3	chr1:223899970-223900553	A549	lung:	n/a	chr1:223900268-223900277
38	ATF3	chr1:223888327-223889401	A549	lung:	n/a	n/a
39	ATF3	chr1:223914178-223914818	K562	blood:	n/a	n/a
40	BACH1	chr1:223914318-223914741	H1-hESC	embryonic stem cell:	n/a	chr1:223914581-223914595
41	BACH1	chr1:223906616-223906885	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr1:223888558-223888931	K562	blood:	n/a	n/a
43	BACH1	chr1:223900029-223900290	H1-hESC	embryonic stem cell:	n/a	n/a
44	BATF	chr1:223914360-223914740	GM12878	blood:	n/a	chr1:223914555-223914566
45	BATF	chr1:223914305-223914788	GM12878	blood:	n/a	chr1:223914555-223914566
46	BCL11A	chr1:223914406-223914693	GM12878	blood:	n/a	chr1:223914507-223914516
47	BCL11A	chr1:223914277-223914798	GM12878	blood:	n/a	chr1:223914507-223914516
48	BCL3	chr1:223914168-223914877	A549	lung:	n/a	chr1:223914507-223914516
49	BCL3	chr1:223894647-223896166	A549	lung:	n/a	n/a
50	BCL3	chr1:223914155-223915090	A549	lung:	n/a	chr1:223914507-223914516

(count:1712 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:223900438-223900488	CMK	blood:	n/a
2	chr1:223889141-223889191	GM12878	blood:	n/a
3	chr1:223903862-223903912	T-47D	breast:	n/a
4	chr1:223899736-223899786	Hela-S3	cervix:	n/a
5	chr1:223900438-223900488	CMK	blood:	n/a
6	chr1:223889141-223889191	GM12878	blood:	n/a
7	chr1:223903862-223903912	T-47D	breast:	n/a
8	chr1:223899736-223899786	Hela-S3	cervix:	n/a
9	chr1:223906133-223906183	HUVEC	blood vessel:	n/a
10	chr1:223903862-223903912	Caco-2	colon:	n/a
11	chr1:223900468-223900518	HRE	kidney:	n/a
12	chr1:223901187-223901237	BJ	skin:	n/a
13	chr1:223899685-223899735	PrEC	prostate:	n/a
14	chr1:223889345-223889395	NH-A	brain:	n/a
15	chr1:223888431-223888481	SK-N-MC	brain:	n/a
16	chr1:223899685-223899735	K562	blood:	n/a
17	chr1:223906133-223906183	AG09319	gingival:	n/a
18	chr1:223899746-223899796	RPTEC	kidney:	n/a
19	chr1:223888905-223888955	HepG2	liver:	n/a
20	chr1:223893441-223893491	A549	lung:	n/a
21	chr1:223897463-223897513	H1-hESC	embryonic stem cell:	embryo
22	chr1:223899736-223899786	NB4	blood:	n/a
23	chr1:223904225-223904275	GM12891	blood:	n/a
24	chr1:223900822-223900872	NHDF-neo	bronchial:	n/a
25	chr1:223901187-223901237	GM06990	blood:	n/a
26	chr1:223888956-223889006	NB4	blood:	n/a
27	chr1:223901187-223901237	Hela-S3	cervix:	n/a
28	chr1:223901187-223901237	HPAEpiC	pulmonary alveolar:	n/a
29	chr1:223919461-223919511	PANC-1	pancreas:	n/a
30	chr1:223901187-223901237	HRCEpiC	kidney:	n/a
31	chr1:223899746-223899796	HNPCEpiC	eye:	n/a
32	chr1:223888869-223888919	Hepatocyte	liver:	n/a
33	chr1:223889345-223889395	CMK	blood:	n/a
34	chr1:223889141-223889191	T-47D	breast:	n/a
35	chr1:223888956-223889006	NHDF-neo	bronchial:	n/a
36	chr1:223899998-223900048	LNCaP	prostate:	n/a
37	chr1:223919461-223919511	AG04450	lung:	fetal
38	chr1:223901187-223901237	HepG2	liver:	n/a
39	chr1:223901187-223901237	HUVEC	blood vessel:	n/a
40	chr1:223897463-223897513	PFSK-1	brain:	n/a
41	chr1:223893441-223893491	HIPEpiC	eye:	n/a
42	chr1:223914343-223914393	Hepatocyte	liver:	n/a
43	chr1:223921358-223921408	HPAEpiC	pulmonary alveolar:	n/a
44	chr1:223888431-223888481	HCM	heart:	n/a
45	chr1:223888869-223888919	SKMC	muscle:	n/a
46	chr1:223899845-223899895	MCF-7	breast:	n/a
47	chr1:223899746-223899796	CMK	blood:	n/a
48	chr1:223899998-223900048	GM19239	blood:	n/a
49	chr1:223900822-223900872	PrEC	prostate:	n/a
50	chr1:223908491-223908541	GM06990	blood:	n/a

(count:137 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:223900092..223902158-chr1:223929992..223931627,2	K562	blood:
2	chr1:223918635..223922245-chr1:223925850..223929641,4	MCF-7	breast:
3	chr1:223886668..223890344-chr1:223897746..223900327,3	K562	blood:
4	chr1:223901725..223903941-chr1:223941728..223943865,2	MCF-7	breast:
5	chr1:223897059..223902247-chr1:223935403..223939761,6	K562	blood:
6	chr1:223693305..223695548-chr1:223894201..223896140,2	MCF-7	breast:
7	chr1:223914360..223914989-chr12:65959195..65960066,2	MCF-7	breast:
8	chr1:223890524..223893483-chr1:223939382..223941203,2	MCF-7	breast:
9	chr1:223919205..223921124-chr1:223921422..223926352,4	K562	blood:
10	chr1:223899965..223900475-chr5:77655637..77656578,2	Hela-S3	cervix:
11	chr1:223893369..223895448-chr1:223913219..223916092,2	K562	blood:
12	chr1:223895120..223895623-chr9:123604912..123605540,2	Hela-S3	cervix:
13	chr1:223898332..223906168-chr1:223910455..223917097,17	K562	blood:
14	chr1:223915826..223918177-chr1:223937169..223939533,2	K562	blood:
15	chr1:223901494..223903169-chr1:223928356..223930429,2	MCF-7	breast:
16	chr1:223906912..223908483-chr1:223923323..223925771,2	MCF-7	breast:
17	chr1:223895202..223897591-chr1:223904463..223906328,2	K562	blood:
18	chr1:223891592..223893967-chr1:223903233..223904840,2	K562	blood:
19	chr1:223908483..223912094-chr1:223930572..223933646,3	MCF-7	breast:
20	chr1:223902474..223903675-chr1:223936616..223937446,3	MCF-7	breast:
21	chr1:223893369..223895448-chr1:223913219..223916092,2	K562	blood:
22	chr1:223904247..223905976-chr1:223916920..223919197,2	MCF-7	breast:
23	chr1:223901394..223904242-chr1:223919607..223921227,2	K562	blood:
24	chr1:223914702..223917591-chr1:223920131..223923452,6	K562	blood:
25	chr1:223887828..223890332-chr1:223892364..223895816,5	K562	blood:
26	chr1:223885961..223896993-chr1:223898177..223910405,32	MCF-7	breast:
27	chr1:223899719..223901460-chr1:224517221..224519970,2	K562	blood:
28	chr1:223885860..223886535-chr1:223897110..223897633,2	MCF-7	breast:
29	chr1:223885547..223886225-chr1:224520929..224521680,2	MCF-7	breast:
30	chr1:223888744..223890349-chr1:223956680..223958231,2	MCF-7	breast:
31	chr1:223898782..223903083-chr1:223918027..223924082,6	K562	blood:
32	chr1:223900203..223902153-chr1:223927273..223928993,2	K562	blood:
33	chr1:223902286..223903884-chr1:223996819..223998348,2	K562	blood:
34	chr1:223884407..223886063-chr1:223901694..223904527,2	K562	blood:
35	chr1:223913473..223915896-chr1:224022022..224024045,2	K562	blood:
36	chr1:223885712..223886555-chr1:224518312..224518842,2	K562	blood:
37	chr1:223907649..223910322-chr1:223936946..223940552,3	MCF-7	breast:
38	chr1:223901244..223903074-chr1:224621960..224624897,2	K562	blood:
39	chr1:223884342..223885890-chr1:223887258..223888847,2	K562	blood:
40	chr1:223893260..223897061-chr1:223935259..223940090,6	MCF-7	breast:
41	chr1:223884342..223885890-chr1:223887258..223888847,2	K562	blood:
42	chr1:223900203..223901722-chr1:223926667..223928773,2	K562	blood:
43	chr1:223894556..223895508-chr10:14920264..14921010,2	HCT-116	colon:
44	chr1:223919304..223920937-chr1:223921422..223924041,2	K562	blood:
45	chr1:223918981..223919488-chr1:223936544..223937377,2	K562	blood:
46	chr1:223899719..223902673-chr1:224516675..224518721,2	K562	blood:
47	chr1:223913291..223915988-chr1:223981454..223983055,2	K562	blood:
48	chr1:223900439..223903816-chr1:223918326..223920507,3	MCF-7	breast:
49	chr1:223887434..223890501-chr1:223901110..223904266,3	K562	blood:
50	chr1:223892791..223896772-chr1:223919510..223922888,4	MCF-7	breast:

No data

Variant related genes	Relation type
CAPN2	TF binding region
CAPN2	CpG island
ENSG00000095261	chromatin interactions
ENSG00000168404	chromatin interactions
ENSG00000272853	chromatin interactions
ENSG00000143537	chromatin interactions
ENSG00000165752	chromatin interactions
ENSG00000143786	chromatin interactions
ENSG00000245556	chromatin interactions
ENSG00000152455	chromatin interactions
ENSG00000143514	chromatin interactions
ENSG00000085365	chromatin interactions
ENSG00000143756	chromatin interactions
ENSG00000119383	chromatin interactions
ENSG00000162923	chromatin interactions
ENSG00000255717	chromatin interactions
ENSG00000143748	chromatin interactions
ENSG00000162909	chromatin interactions
ENSG00000168003	chromatin interactions
ENSG00000203697	chromatin interactions
ENSG00000148814	chromatin interactions
ENSG00000226752	chromatin interactions

Extended variants
information (count: 1432 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1432 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2000319	chr1:223885843-223885844	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542615141	chr1:223885861-223885862	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs112351897	chr1:223885873-223885874	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs560911086	chr1:223885907-223885908	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs6677286	chr1:223885910-223885911	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs368292845	chr1:223885959-223885960	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs541521997	chr1:223886029-223886030	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs371574882	chr1:223886055-223886056	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs541768973	chr1:223886077-223886078	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs372015180	chr1:223886090-223886091	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs551698664	chr1:223886133-223886134	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs560187810	chr1:223886153-223886154	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs561693695	chr1:223886178-223886179	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs148770112	chr1:223886235-223886236	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs549017363	chr1:223886265-223886266	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs189412524	chr1:223886299-223886300	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs17556764	chr1:223886321-223886322	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs549596550	chr1:223886338-223886339	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs571851940	chr1:223886384-223886385	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs369116163	chr1:223886385-223886386	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs534722311	chr1:223886393-223886394	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs181823510	chr1:223886432-223886433	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs185403321	chr1:223886435-223886436	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs554570392	chr1:223886468-223886469	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs576012543	chr1:223886489-223886490	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs145001175	chr1:223886515-223886516	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs564152031	chr1:223886516-223886517	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs188105349	chr1:223886530-223886531	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs577217096	chr1:223886552-223886553	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs181313363	chr1:223886567-223886568	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs560257360	chr1:223886582-223886583	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs186495051	chr1:223886601-223886602	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs149332934	chr1:223886676-223886677	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs564255393	chr1:223886700-223886701	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs560902921	chr1:223886704-223886705	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs116078019	chr1:223886725-223886726	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs549895682	chr1:223886761-223886762	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs386639758	chr1:223886770-223886771	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs6699830	chr1:223886784-223886785	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs6702314	chr1:223886822-223886823	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs370766920	chr1:223886835-223886836	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs68100907	chr1:223886836-223886837	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs386369760	chr1:223886845-223886846	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs57194157	chr1:223886850-223886851	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs6688228	chr1:223886851-223886852	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs6680724	chr1:223886855-223886856	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs375412941	chr1:223886932-223886933	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs35616426	chr1:223886939-223886940	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs6702430	chr1:223886946-223886947	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs191702138	chr1:223887153-223887154	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	20808228	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2805 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223881800-223887000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr1:223883600-223887800	Weak transcription	Fetal Intestine Small	intestine
3	chr1:223883800-223887600	Weak transcription	Fetal Intestine Large	intestine
4	chr1:223884000-223888400	Weak transcription	Right Atrium	heart
5	chr1:223884200-223886200	Weak transcription	NH-A	brain
6	chr1:223884200-223887600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr1:223884200-223888000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:223884400-223886200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr1:223884400-223886200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr1:223884400-223886400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr1:223884400-223887400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr1:223884400-223888400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr1:223884400-223888800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:223884400-223888800	Weak transcription	Pancreas	Pancrea
15	chr1:223884600-223886800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr1:223884800-223886000	Weak transcription	Primary B cells from peripheral blood	blood
17	chr1:223885600-223886000	Enhancers	Brain Angular Gyrus	brain
18	chr1:223885600-223886000	Enhancers	Brain Anterior Caudate	brain
19	chr1:223885600-223886200	Enhancers	NHLF	lung
20	chr1:223885600-223886400	Enhancers	Brain Cingulate Gyrus	brain
21	chr1:223885600-223886400	Enhancers	Brain Substantia Nigra	brain
22	chr1:223885600-223886400	Enhancers	HUVEC	blood vessel
23	chr1:223885600-223886600	Enhancers	Primary T cells fromperipheralblood	blood
24	chr1:223885600-223886600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:223885600-223887400	Enhancers	A549	lung
26	chr1:223885600-223888400	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr1:223885800-223886400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr1:223885800-223886400	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr1:223885800-223886400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr1:223885800-223886400	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr1:223885800-223886400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr1:223885800-223886400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr1:223885800-223886400	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr1:223885800-223886400	Enhancers	Adipose Nuclei	Adipose
35	chr1:223885800-223886400	Flanking Active TSS	Brain Hippocampus Middle	brain
36	chr1:223885800-223886400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
37	chr1:223885800-223886400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
38	chr1:223885800-223886400	Enhancers	GM12878-XiMat	blood
39	chr1:223885800-223886400	Enhancers	HSMM	muscle
40	chr1:223885800-223886600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr1:223885800-223886600	Enhancers	Muscle Satellite Cultured Cells	--
42	chr1:223885800-223886600	Enhancers	K562	blood
43	chr1:223885800-223886600	Enhancers	Osteobl	bone
44	chr1:223885800-223887400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr1:223885800-223887800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr1:223885800-223888600	Enhancers	NHDF-Ad	bronchial
47	chr1:223886000-223886200	Flanking Active TSS	Brain Anterior Caudate	brain
48	chr1:223886000-223886200	Enhancers	Fetal Muscle Trunk	muscle
49	chr1:223886000-223886200	Enhancers	Ovary	ovary
50	chr1:223886000-223886200	Active TSS	Stomach Smooth Muscle	stomach

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