Variant report

Variant	nsv872545
Chromosome Location	chr1:171735198-171805448
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1412)
CpG islands
(count:1283)
Chromatin interactive
region (count:91)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1412 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:171786693-171786947	K562	blood:	n/a	n/a
2	ARID3A	chr1:171749992-171750949	K562	blood:	n/a	n/a
3	ARID3A	chr1:171746780-171746789	K562	blood:	n/a	n/a
4	ARID3A	chr1:171786817-171787048	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:171750045-171750820	HepG2	liver:	n/a	n/a
6	ATF1	chr1:171768486-171768546	K562	blood:	n/a	n/a
7	ATF1	chr1:171786560-171787166	K562	blood:	n/a	n/a
8	ATF1	chr1:171797978-171798178	K562	blood:	n/a	n/a
9	ATF1	chr1:171763226-171763571	K562	blood:	n/a	n/a
10	ATF1	chr1:171750164-171751030	K562	blood:	n/a	n/a
11	ATF2	chr1:171750327-171750781	GM12878	blood:	n/a	n/a
12	ATF2	chr1:171750032-171751027	GM12878	blood:	n/a	n/a
13	ATF2	chr1:171750215-171750730	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr1:171750151-171750960	K562	blood:	n/a	n/a
15	ATF3	chr1:171786812-171787102	K562	blood:	n/a	n/a
16	BACH1	chr1:171750805-171751112	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr1:171750084-171750362	K562	blood:	n/a	n/a
18	BACH1	chr1:171738354-171738672	K562	blood:	n/a	n/a
19	BACH1	chr1:171786859-171787163	H1-hESC	embryonic stem cell:	n/a	chr1:171787012-171787026
20	BACH1	chr1:171738264-171738602	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr1:171786843-171787058	GM12878	blood:	n/a	chr1:171786974-171786985
22	BATF	chr1:171774968-171775212	GM12878	blood:	n/a	n/a
23	BATF	chr1:171774999-171775265	GM12878	blood:	n/a	n/a
24	BCL3	chr1:171750054-171751171	A549	lung:	n/a	chr1:171750264-171750277 chr1:171750404-171750417
25	BCLAF1	chr1:171750111-171751116	GM12878	blood:	n/a	chr1:171750264-171750277 chr1:171750404-171750417
26	BDP1	chr1:171770654-171771081	Hela-S3	cervix:	n/a	n/a
27	BHLHE40	chr1:171749999-171751250	K562	blood:	n/a	n/a
28	BHLHE40	chr1:171746537-171746826	K562	blood:	n/a	n/a
29	BHLHE40	chr1:171750125-171751177	GM12878	blood:	n/a	n/a
30	BHLHE40	chr1:171750224-171750946	HepG2	liver:	n/a	n/a
31	BHLHE40	chr1:171768779-171768789	K562	blood:	n/a	n/a
32	BHLHE40	chr1:171786625-171787184	K562	blood:	n/a	n/a
33	BHLHE40	chr1:171770362-171770904	K562	blood:	n/a	n/a
34	BHLHE40	chr1:171770600-171770800	GM12878	blood:	n/a	n/a
35	BRCA1	chr1:171750076-171750990	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr1:171750008-171750957	K562	blood:	n/a	n/a
37	CBX3	chr1:171796096-171796486	K562	blood:	n/a	n/a
38	CBX3	chr1:171749560-171751124	K562	blood:	n/a	n/a
39	CBX3	chr1:171797993-171798265	K562	blood:	n/a	n/a
40	CCNT2	chr1:171786602-171787059	K562	blood:	n/a	n/a
41	CCNT2	chr1:171750192-171751000	K562	blood:	n/a	n/a
42	CEBPB	chr1:171786833-171787483	A549	lung:	n/a	chr1:171787280-171787291
43	CEBPB	chr1:171748609-171748934	H1-hESC	embryonic stem cell:	n/a	chr1:171748797-171748808
44	CEBPB	chr1:171792678-171792897	A549	lung:	n/a	chr1:171792789-171792800 chr1:171792790-171792799
45	CEBPB	chr1:171779076-171779262	IMR90	lung:	n/a	n/a
46	CEBPB	chr1:171742000-171742364	K562	blood:	n/a	chr1:171742176-171742187
47	CEBPB	chr1:171792703-171792902	K562	blood:	n/a	chr1:171792789-171792800 chr1:171792790-171792799
48	CEBPB	chr1:171737821-171738118	K562	blood:	n/a	chr1:171737971-171737984
49	CEBPB	chr1:171769438-171769601	A549	lung:	n/a	n/a
50	CEBPB	chr1:171750078-171751294	Hela-S3	cervix:	n/a	chr1:171750715-171750723

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:171750545-171750595	NT2-D1	testis:	n/a
2	chr1:171770825-171770875	A549	lung:	n/a
3	chr1:171750545-171750595	NT2-D1	testis:	n/a
4	chr1:171770825-171770875	A549	lung:	n/a
5	chr1:171755066-171755116	GM12891	blood:	n/a
6	chr1:171750926-171750976	HMEC	breast:	n/a
7	chr1:171750281-171750331	BJ	skin:	n/a
8	chr1:171750545-171750595	Hela-S3	cervix:	n/a
9	chr1:171750566-171750616	NT2-D1	testis:	n/a
10	chr1:171770825-171770875	H1-hESC	embryonic stem cell:	embryo
11	chr1:171750693-171750743	T-47D	breast:	n/a
12	chr1:171750797-171750847	U87	brain:	n/a
13	chr1:171750782-171750832	SK-N-MC	brain:	n/a
14	chr1:171750547-171750597	GM12892	blood:	n/a
15	chr1:171753185-171753235	IMR90	lung:	fetal
16	chr1:171765992-171766042	LNCaP	prostate:	n/a
17	chr1:171750547-171750597	GM19239	blood:	n/a
18	chr1:171753185-171753235	PFSK-1	brain:	n/a
19	chr1:171755066-171755116	HUVEC	blood vessel:	n/a
20	chr1:171750926-171750976	AG04450	lung:	fetal
21	chr1:171750547-171750597	T-47D	breast:	n/a
22	chr1:171765992-171766042	NT2-D1	testis:	n/a
23	chr1:171756153-171756203	HIPEpiC	eye:	n/a
24	chr1:171750797-171750847	AG10803	skin:	n/a
25	chr1:171750545-171750595	HUVEC	blood vessel:	n/a
26	chr1:171753628-171753678	NT2-D1	testis:	n/a
27	chr1:171753628-171753678	NHBE	bronchial:	n/a
28	chr1:171753628-171753678	CMK	blood:	n/a
29	chr1:171751291-171751341	HEEpiC	esophagus:	n/a
30	chr1:171787181-171787231	BJ	skin:	n/a
31	chr1:171750281-171750331	U87	brain:	n/a
32	chr1:171756153-171756203	AG04449	skin:	fetal
33	chr1:171753185-171753235	HRCEpiC	kidney:	n/a
34	chr1:171750782-171750832	HCT-116	colon:	n/a
35	chr1:171750501-171750551	HRCEpiC	kidney:	n/a
36	chr1:171750797-171750847	MCF10A-Er-Src	breast:	n/a
37	chr1:171770825-171770875	HNPCEpiC	eye:	n/a
38	chr1:171750501-171750551	AG04449	skin:	fetal
39	chr1:171750545-171750595	HMEC	breast:	n/a
40	chr1:171755066-171755116	AG04450	lung:	fetal
41	chr1:171765992-171766042	HRCEpiC	kidney:	n/a
42	chr1:171751291-171751341	PFSK-1	brain:	n/a
43	chr1:171753628-171753678	AG04449	skin:	fetal
44	chr1:171747089-171747139	NB4	blood:	n/a
45	chr1:171750547-171750597	PFSK-1	brain:	n/a
46	chr1:171750281-171750331	GM12892	blood:	n/a
47	chr1:171750566-171750616	SK-N-MC	brain:	n/a
48	chr1:171750545-171750595	HAEpiC	amniotic membrane:	n/a
49	chr1:171756153-171756203	AG09309	skin:	n/a
50	chr1:171750693-171750743	AG10803	skin:	n/a

(count:91 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:171710046..171714350-chr1:171748592..171750523,6	K562	blood:
2	chr1:171771604..171774137-chr1:171780038..171783681,3	MCF-7	breast:
3	chr1:171749924..171750607-chr10:105211765..105212634,2	HCT-116	colon:
4	chr1:171710341..171715416-chr1:171748571..171752440,7	MCF-7	breast:
5	chr1:171730299..171731843-chr1:171736543..171739308,2	K562	blood:
6	chr1:171768042..171770155-chr1:171772867..171774422,2	MCF-7	breast:
7	chr1:171738907..171740950-chr1:171747822..171750244,2	MCF-7	breast:
8	chr1:171760261..171763188-chr1:171766979..171768595,2	MCF-7	breast:
9	chr1:171749779..171754190-chr1:171762974..171767849,5	K562	blood:
10	chr1:171750745..171751328-chr6:7910543..7911467,2	NB4	blood:
11	chr1:171754075..171756411-chr1:171764040..171766145,2	MCF-7	breast:
12	chr1:171738793..171742009-chr1:171745293..171748243,3	K562	blood:
13	chr1:171785613..171787627-chr1:171789053..171791436,2	K562	blood:
14	chr1:171709904..171712357-chr1:171759667..171762572,3	K562	blood:
15	chr1:171729687..171733295-chr1:171747531..171751881,5	K562	blood:
16	chr1:171738704..171740744-chr1:171745299..171748129,2	MCF-7	breast:
17	chr1:171749779..171754190-chr1:171762974..171767849,5	K562	blood:
18	chr1:171764717..171768373-chr1:171769892..171773572,7	K562	blood:
19	chr1:171750053..171752040-chr1:171760205..171763597,3	MCF-7	breast:
20	chr1:171735538..171739658-chr1:171748409..171750930,4	MCF-7	breast:
21	chr1:171710037..171714996-chr1:171734843..171738629,6	MCF-7	breast:
22	chr1:171804485..171806201-chr1:171808238..171810871,2	MCF-7	breast:
23	chr1:171754075..171756411-chr1:171764040..171766145,2	MCF-7	breast:
24	chr1:171712949..171715185-chr1:171753608..171756289,2	K562	blood:
25	chr1:171802586..171806462-chr1:171808258..171810668,4	K562	blood:
26	chr1:171748445..171750403-chr1:173987079..173989780,2	MCF-7	breast:
27	chr1:171746858..171748372-chr1:171748853..171751746,3	K562	blood:
28	chr1:171749390..171751584-chr1:171778813..171780615,2	MCF-7	breast:
29	chr1:171755451..171759519-chr1:171762178..171766070,4	MCF-7	breast:
30	chr1:171738793..171742009-chr1:171745293..171748243,3	K562	blood:
31	chr1:171710045..171712872-chr1:171732812..171737029,6	MCF-7	breast:
32	chr1:171769639..171771616-chr1:171952138..171953508,27	MCF-7	breast:
33	chr1:171709564..171713750-chr1:171736602..171743117,7	K562	blood:
34	chr1:171734176..171737844-chr1:171748206..171752284,5	K562	blood:
35	chr1:171710019..171713750-chr1:171741617..171744862,3	K562	blood:
36	chr1:171760261..171763188-chr1:171766979..171768595,2	MCF-7	breast:
37	chr1:171771604..171774137-chr1:171780038..171783681,3	MCF-7	breast:
38	chr1:171787129..171789980-chr1:171790659..171793277,3	MCF-7	breast:
39	chr1:171768042..171770155-chr1:171772867..171774422,2	MCF-7	breast:
40	chr1:171709806..171712029-chr1:171768013..171770054,2	MCF-7	breast:
41	chr1:171734034..171736178-chr1:171746102..171748315,3	K562	blood:
42	chr1:171785613..171787627-chr1:171789053..171791436,2	K562	blood:
43	chr1:171770037..171771242-chr1:171953555..171955020,9	MCF-7	breast:
44	chr1:171750345..171750984-chr19:56146237..56147133,2	Hela-S3	cervix:
45	chr1:171724145..171725831-chr1:171749285..171750823,2	K562	blood:
46	chr1:171738743..171740462-chr1:171742324..171745005,2	K562	blood:
47	chr1:171769328..171770170-chr1:171952653..171953200,2	MCF-7	breast:
48	chr1:171738704..171740744-chr1:171745299..171748129,2	MCF-7	breast:
49	chr1:171755758..171758426-chr1:171775060..171777490,2	MCF-7	breast:
50	chr1:171785258..171787192-chr1:171953083..171954912,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-METTL13-3	chr1:171748117-171748192	NONHSAT007582
2	lnc-METTL13-3	chr1:171750371-171750648	NONHSAT007582

No data

Variant related genes	Relation type
METTL13	TF binding region
ENSG00000253060	TF binding region
ENSG00000213060	TF binding region
ENSG00000252134	TF binding region
ENSG00000224600	TF binding region
METTL13	CpG island
ENSG00000253060	CpG island
ENSG00000213060	CpG island
ENSG00000252134	CpG island
ENSG00000224600	CpG island
ENSG00000239264	chromatin interactions
ENSG00000213015	chromatin interactions
ENSG00000252134	chromatin interactions
ENSG00000010165	chromatin interactions
ENSG00000117533	chromatin interactions
ENSG00000224600	chromatin interactions
ENSG00000232261	chromatin interactions
ENSG00000226609	chromatin interactions
ENSG00000149218	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000197959	chromatin interactions
ENSG00000213060	chromatin interactions
ENSG00000171425	chromatin interactions
ENSG00000253060	chromatin interactions
ENSG00000138172	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000180992	chromatin interactions
ENSG00000236741	chromatin interactions
ENSG00000137216	chromatin interactions
ENSG00000234699	chromatin interactions
ENSG00000271459	chromatin interactions

Extended variants
information (count: 2758 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2758 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12032340	chr1:171735198-171735199	Inactive region	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs12028128	chr1:171735205-171735206	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs373653972	chr1:171735209-171735210	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs572956082	chr1:171735267-171735268	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs142853524	chr1:171735376-171735377	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs561660927	chr1:171735425-171735426	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs113315871	chr1:171735447-171735448	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs544499140	chr1:171735496-171735497	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs146215968	chr1:171735560-171735561	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs562601882	chr1:171735563-171735564	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs533168133	chr1:171735574-171735575	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs551259636	chr1:171735575-171735576	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs12127193	chr1:171735588-171735589	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs564268542	chr1:171735602-171735603	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs12127217	chr1:171735639-171735640	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs528548918	chr1:171735657-171735658	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs7542116	chr1:171735666-171735667	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs151039338	chr1:171735686-171735687	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs140911113	chr1:171735693-171735694	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs551262324	chr1:171735716-171735717	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs569413735	chr1:171735720-171735721	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs190898196	chr1:171735726-171735727	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs78251655	chr1:171735784-171735785	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs566613234	chr1:171735803-171735804	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs533872033	chr1:171735858-171735859	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs144107327	chr1:171735874-171735875	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs7551037	chr1:171735909-171735910	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs138969294	chr1:171735975-171735976	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs552307877	chr1:171736001-171736002	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs547182785	chr1:171736008-171736009	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs6689125	chr1:171736037-171736038	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs12127345	chr1:171736087-171736088	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs67298573	chr1:171736137-171736138	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs71823398	chr1:171736139-171736140	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs559904787	chr1:171736147-171736148	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs528608718	chr1:171736164-171736165	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs12072468	chr1:171736168-171736169	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs568908180	chr1:171736222-171736223	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs7542691	chr1:171736254-171736255	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs112401057	chr1:171736255-171736256	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs561802626	chr1:171736280-171736281	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs529302019	chr1:171736310-171736311	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs185556368	chr1:171736316-171736317	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs373445879	chr1:171736327-171736328	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs569570351	chr1:171736376-171736377	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs114595164	chr1:171736386-171736387	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs76742536	chr1:171736399-171736400	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs183155539	chr1:171736415-171736416	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs534349666	chr1:171736421-171736422	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs555516921	chr1:171736452-171736453	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
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
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	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
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	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
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	20409316	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1623 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:171735200-171735400	Enhancers	Monocytes-CD14+_RO01746	blood
2	chr1:171735200-171738600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr1:171735400-171735800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr1:171735800-171736000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr1:171735800-171736000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:171735800-171736200	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr1:171736200-171736600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr1:171736600-171736800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr1:171736600-171737000	Enhancers	Adipose Nuclei	Adipose
10	chr1:171736600-171738600	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr1:171736800-171737400	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr1:171737000-171737400	Weak transcription	Adipose Nuclei	Adipose
13	chr1:171737400-171738200	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr1:171737400-171738600	Enhancers	Adipose Nuclei	Adipose
15	chr1:171737600-171738400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr1:171737600-171739200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr1:171737800-171739200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:171737800-171739200	Enhancers	Fetal Brain Male	brain
19	chr1:171737800-171739200	Enhancers	Fetal Brain Female	brain
20	chr1:171738400-171739400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr1:171738600-171741600	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr1:171738600-171741600	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr1:171739400-171740000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr1:171739400-171744400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:171740000-171749800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr1:171741400-171742400	Enhancers	Primary B cells from cord blood	blood
27	chr1:171741600-171742000	Enhancers	GM12878-XiMat	blood
28	chr1:171741600-171742400	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr1:171741600-171742600	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr1:171744400-171745400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr1:171745400-171749400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:171746400-171746600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr1:171746400-171747200	Enhancers	K562	blood
34	chr1:171746600-171747000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:171746600-171747200	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr1:171747000-171749400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr1:171747200-171748400	Weak transcription	K562	blood
38	chr1:171747200-171749400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr1:171747600-171749600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr1:171748400-171749400	Enhancers	K562	blood
41	chr1:171748800-171749000	Enhancers	Dnd41	blood
42	chr1:171749000-171749600	Enhancers	Brain Germinal Matrix	brain
43	chr1:171749000-171749800	Enhancers	Primary T cells fromperipheralblood	blood
44	chr1:171749000-171749800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr1:171749000-171750200	Flanking Active TSS	Dnd41	blood
46	chr1:171749200-171749400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr1:171749200-171749400	Enhancers	Colon Smooth Muscle	Colon
48	chr1:171749200-171749600	Enhancers	Primary T helper naive cells from peripheral blood	blood
49	chr1:171749200-171749600	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr1:171749200-171749600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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