Variant report

Variant	nsv883218
Chromosome Location	chr5:178219855-178349391
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1635)
CpG islands
(count:2139)
Chromatin interactive
region (count:81)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1635 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178266442-178266591	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:178286713-178287002	HepG2	liver:	n/a	n/a
3	ATF1	chr5:178286762-178287220	K562	blood:	n/a	n/a
4	ATF1	chr5:178265901-178266202	K562	blood:	n/a	n/a
5	ATF2	chr5:178286589-178286974	GM12878	blood:	n/a	n/a
6	ATF3	chr5:178286654-178287084	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr5:178286755-178287144	K562	blood:	n/a	n/a
8	BACH1	chr5:178259949-178259966	K562	blood:	n/a	n/a
9	BACH1	chr5:178286831-178287481	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:178254765-178254792	K562	blood:	n/a	n/a
11	BACH1	chr5:178322769-178323665	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:178299171-178299685	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr5:178315712-178315791	K562	blood:	n/a	n/a
14	BACH1	chr5:178299147-178299711	K562	blood:	n/a	n/a
15	BCL3	chr5:178220955-178221285	GM12878	blood:	n/a	n/a
16	BCLAF1	chr5:178286652-178287189	GM12878	blood:	n/a	n/a
17	BCLAF1	chr5:178286705-178287046	K562	blood:	n/a	n/a
18	BCLAF1	chr5:178286646-178287185	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:178223850-178223909	K562	blood:	n/a	chr5:178223892-178223901 chr5:178223891-178223900 chr5:178223893-178223902 chr5:178223892-178223901
20	BHLHE40	chr5:178317264-178317357	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:178281355-178281697	K562	blood:	n/a	n/a
22	BHLHE40	chr5:178286636-178287416	K562	blood:	n/a	chr5:178287282-178287298 chr5:178287277-178287293
23	BHLHE40	chr5:178266434-178266669	K562	blood:	n/a	n/a
24	BHLHE40	chr5:178281482-178281689	HepG2	liver:	n/a	n/a
25	BHLHE40	chr5:178266386-178266649	HepG2	liver:	n/a	n/a
26	BHLHE40	chr5:178223819-178224462	GM12878	blood:	n/a	chr5:178223892-178223901 chr5:178223891-178223900 chr5:178223893-178223902 chr5:178223892-178223901
27	BHLHE40	chr5:178286715-178287439	HepG2	liver:	n/a	chr5:178287282-178287298 chr5:178287277-178287293
28	BHLHE40	chr5:178259661-178259927	K562	blood:	n/a	n/a
29	BHLHE40	chr5:178286530-178287352	GM12878	blood:	n/a	chr5:178287282-178287298 chr5:178287277-178287293
30	BHLHE40	chr5:178322756-178322977	GM12878	blood:	n/a	n/a
31	BRCA1	chr5:178286778-178287148	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr5:178286775-178286962	HepG2	liver:	n/a	n/a
33	BRCA1	chr5:178266539-178266607	HepG2	liver:	n/a	n/a
34	CBX3	chr5:178286622-178287208	K562	blood:	n/a	n/a
35	CBX3	chr5:178336274-178336602	K562	blood:	n/a	n/a
36	CBX3	chr5:178286504-178287357	HCT-116	colon:	n/a	n/a
37	CBX3	chr5:178310545-178310982	K562	blood:	n/a	n/a
38	CBX3	chr5:178310127-178310478	K562	blood:	n/a	n/a
39	CCNT2	chr5:178281392-178281608	K562	blood:	n/a	n/a
40	CCNT2	chr5:178286759-178287496	K562	blood:	n/a	n/a
41	CEBPB	chr5:178257724-178257754	HepG2	liver:	n/a	n/a
42	CEBPB	chr5:178231520-178231709	HepG2	liver:	n/a	chr5:178231622-178231633
43	CEBPB	chr5:178329808-178330264	Hela-S3	cervix:	n/a	chr5:178329882-178329893
44	CEBPB	chr5:178333052-178333243	HepG2	liver:	n/a	chr5:178333136-178333147
45	CEBPB	chr5:178322299-178322989	Hela-S3	cervix:	n/a	chr5:178322475-178322486
46	CEBPB	chr5:178325229-178325551	IMR90	lung:	n/a	chr5:178325383-178325394 chr5:178325382-178325393
47	CEBPB	chr5:178322401-178322967	H1-hESC	embryonic stem cell:	n/a	chr5:178322475-178322486
48	CEBPB	chr5:178285796-178285889	K562	blood:	n/a	n/a
49	CEBPB	chr5:178325294-178325515	Hela-S3	cervix:	n/a	chr5:178325383-178325394 chr5:178325382-178325393
50	CEBPB	chr5:178286811-178287376	Hela-S3	cervix:	n/a	n/a

(count:2139 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178220238-178220288	HEEpiC	esophagus:	n/a
2	chr5:178322737-178322787	ovcar-3	ovarian:	n/a
3	chr5:178288625-178288675	HepG2	liver:	n/a
4	chr5:178288625-178288675	PANC-1	pancreas:	n/a
5	chr5:178220238-178220288	HEEpiC	esophagus:	n/a
6	chr5:178322737-178322787	ovcar-3	ovarian:	n/a
7	chr5:178288625-178288675	HepG2	liver:	n/a
8	chr5:178288625-178288675	PANC-1	pancreas:	n/a
9	chr5:178287767-178287817	MCF10A-Er-Src	breast:	n/a
10	chr5:178287445-178287495	AG10803	skin:	n/a
11	chr5:178286920-178286970	GM12891	blood:	n/a
12	chr5:178286881-178286931	AG04450	lung:	fetal
13	chr5:178339353-178339403	SK-N-MC	brain:	n/a
14	chr5:178322737-178322787	SK-N-SH_RA	brain:	n/a
15	chr5:178339353-178339403	HAEpiC	amniotic membrane:	n/a
16	chr5:178220967-178221017	ovcar-3	ovarian:	n/a
17	chr5:178327314-178327364	SAEC	small airway:	n/a
18	chr5:178286881-178286931	AG04449	skin:	fetal
19	chr5:178288625-178288675	PFSK-1	brain:	n/a
20	chr5:178286881-178286931	K562	blood:	n/a
21	chr5:178286920-178286970	HUVEC	blood vessel:	n/a
22	chr5:178286735-178286785	U87	brain:	n/a
23	chr5:178286875-178286925	HCM	heart:	n/a
24	chr5:178288650-178288700	MCF-7	breast:	n/a
25	chr5:178286920-178286970	Hepatocyte	liver:	n/a
26	chr5:178266137-178266187	SK-N-MC	brain:	n/a
27	chr5:178287767-178287817	AG04450	lung:	fetal
28	chr5:178322856-178322906	AG04450	lung:	fetal
29	chr5:178266060-178266110	HRCEpiC	kidney:	n/a
30	chr5:178283861-178283911	HEEpiC	esophagus:	n/a
31	chr5:178291250-178291300	PrEC	prostate:	n/a
32	chr5:178339445-178339495	SK-N-MC	brain:	n/a
33	chr5:178286857-178286907	PrEC	prostate:	n/a
34	chr5:178322792-178322842	NB4	blood:	n/a
35	chr5:178322752-178322802	HPAEpiC	pulmonary alveolar:	n/a
36	chr5:178339445-178339495	ECC-1	luminal epithelium:	n/a
37	chr5:178287544-178287594	SAEC	small airway:	n/a
38	chr5:178286920-178286970	AG04450	lung:	fetal
39	chr5:178266137-178266187	ProgFib	skin:	n/a
40	chr5:178322737-178322787	SAEC	small airway:	n/a
41	chr5:178246278-178246328	HCT-116	colon:	n/a
42	chr5:178286875-178286925	CMK	blood:	n/a
43	chr5:178266060-178266110	K562	blood:	n/a
44	chr5:178322856-178322906	HCT-116	colon:	n/a
45	chr5:178322924-178322974	RPTEC	kidney:	n/a
46	chr5:178288650-178288700	GM12892	blood:	n/a
47	chr5:178286892-178286942	HEEpiC	esophagus:	n/a
48	chr5:178322737-178322787	HCT-116	colon:	n/a
49	chr5:178266175-178266225	T-47D	breast:	n/a
50	chr5:178339172-178339222	HEK293	kidney:	embryo

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:178251204..178253302-chr5:178256012..178257744,2	MCF-7	breast:
2	chr5:178310967..178313055-chr5:178314057..178317226,3	MCF-7	breast:
3	chr13:38619618..38620640-chr5:178301624..178302148,7	MCF-7	breast:
4	chr5:178219935..178220578-chr5:178266097..178266710,3	MCF-7	breast:
5	chr5:178299499..178302283-chr5:178303072..178304596,2	MCF-7	breast:
6	chr5:178219952..178220766-chr5:178688074..178688887,3	MCF-7	breast:
7	chr5:178223973..178226497-chr5:178266303..178268866,2	MCF-7	breast:
8	chr5:178306684..178308564-chr5:178323715..178325258,2	MCF-7	breast:
9	chr5:178276049..178278354-chr5:178322079..178324403,2	MCF-7	breast:
10	chr5:178285700..178288538-chr5:178289208..178291375,4	MCF-7	breast:
11	chr5:178262543..178264784-chr5:178273613..178275521,2	K562	blood:
12	chr5:178290096..178292803-chr5:178294356..178296794,2	K562	blood:
13	chr5:178248233..178250497-chr5:178253238..178254765,2	K562	blood:
14	chr5:177640785..177642286-chr5:178288319..178291268,2	K562	blood:
15	chr5:178286202..178288333-chr5:178295235..178296864,2	MCF-7	breast:
16	chr5:178157230..178157844-chr5:178286636..178287441,3	MCF-7	breast:
17	chr5:177661196..177662135-chr5:178266134..178266915,2	MCF-7	breast:
18	chr5:178251481..178253894-chr5:178255525..178257493,2	K562	blood:
19	chr5:178214124..178214763-chr5:178265905..178266637,2	MCF-7	breast:
20	chr5:178286798..178288918-chr5:178487242..178488938,2	MCF-7	breast:
21	chr5:178252394..178254113-chr5:178255346..178258174,3	K562	blood:
22	chr5:178157446..178157947-chr5:178286420..178286940,2	MCF-7	breast:
23	chr5:178279881..178281408-chr5:178284466..178287127,2	MCF-7	breast:
24	chr5:178299499..178302283-chr5:178303072..178304596,2	MCF-7	breast:
25	chr5:178262543..178264784-chr5:178273613..178275521,2	K562	blood:
26	chr5:177706663..177708953-chr5:178261165..178263624,2	MCF-7	breast:
27	chr5:178228775..178231759-chr5:178257850..178260513,2	MCF-7	breast:
28	chr5:178315972..178317729-chr5:178321296..178324205,3	MCF-7	breast:
29	chr5:178285911..178288443-chr5:178294689..178296630,2	K562	blood:
30	chr5:178285646..178289279-chr5:178321547..178324884,4	MCF-7	breast:
31	chr5:178264186..178266313-chr5:178270488..178273068,2	MCF-7	breast:
32	chr5:178219922..178220838-chr5:178920668..178921270,2	MCF-7	breast:
33	chr5:178156362..178158364-chr5:178252776..178254974,2	K562	blood:
34	chr5:178258610..178261483-chr5:178285999..178288925,2	K562	blood:
35	chr5:178264186..178266313-chr5:178270488..178273068,2	MCF-7	breast:
36	chr5:178157412..178158250-chr5:178286406..178286923,4	MCF-7	breast:
37	chr5:178306684..178308564-chr5:178323715..178325258,2	MCF-7	breast:
38	chr5:178157367..178158168-chr5:178266123..178266937,3	MCF-7	breast:
39	chr5:178256899..178257517-chr5:178489612..178490272,2	K562	blood:
40	chr5:178156014..178158845-chr5:178285994..178289826,5	MCF-7	breast:
41	chr5:178314966..178317801-chr5:178321245..178325821,5	MCF-7	breast:
42	chr5:178219935..178220578-chr5:178266097..178266710,3	MCF-7	breast:
43	chr5:178285493..178288791-chr5:178303197..178305318,3	MCF-7	breast:
44	chr5:178322017..178324460-chr5:178337015..178339677,2	MCF-7	breast:
45	chr5:178324334..178326418-chr5:178335750..178338330,2	K562	blood:
46	chr5:178157243..178158078-chr5:178286943..178287443,2	MCF-7	breast:
47	chr5:178250159..178253046-chr5:178256116..178259012,3	MCF-7	breast:
48	chr5:178228775..178231759-chr5:178257850..178260513,2	MCF-7	breast:
49	chr5:178211735..178215494-chr5:178218190..178221753,4	MCF-7	breast:
50	chr5:178053047..178055636-chr5:178260492..178262068,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF354B-1	chr5:178312488-178312734	NONHSAT105561
2	lnc-ZNF454-2	chr5:178349065-178349717	NONHSAT105562
3	lnc-ZNF354B-1	chr5:178311168-178311519	NONHSAT105559
4	lnc-ZNF354B-1	chr5:178312615-178312734	NONHSAT105559
5	lnc-ZNF354B-1	chr5:178314610-178314887	NONHSAT105561
6	lnc-ZNF354B-1	chr5:178314610-178315123	NONHSAT105559

No data

Variant related genes	Relation type
ZFP2	TF binding region
PIGFP1	TF binding region
RNU1-39P	TF binding region
ENSG00000253725	TF binding region
ZNF354B	TF binding region
AACSP1	TF binding region
ENSG00000213328	TF binding region
ZFP2	CpG island
PIGFP1	CpG island
RNU1-39P	CpG island
ENSG00000253725	CpG island
ZNF354B	CpG island
AACSP1	CpG island
ENSG00000213328	CpG island
ENSG00000169131	chromatin interactions
ENSG00000198939	chromatin interactions
ENSG00000213328	chromatin interactions
ENSG00000177932	chromatin interactions
ENSG00000206624	chromatin interactions
ENSG00000113240	chromatin interactions
ENSG00000178338	chromatin interactions
ENSG00000250420	chromatin interactions
ENSG00000253725	chromatin interactions

Extended variants
information (count: 6399 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:6399 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7711944	chr5:178219855-178219856	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs62393906	chr5:178219914-178219915	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs562028837	chr5:178219915-178219916	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs374734516	chr5:178219923-178219924	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs190727749	chr5:178219952-178219953	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs559502945	chr5:178219967-178219968	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs143912943	chr5:178219968-178219969	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs551585653	chr5:178219976-178219977	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs7713247	chr5:178219977-178219978	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs370759367	chr5:178219985-178219986	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs537231969	chr5:178219987-178219988	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs371955519	chr5:178219992-178219993	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs201800993	chr5:178220000-178220001	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs62393907	chr5:178220024-178220025	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs567541396	chr5:178220062-178220063	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs144262390	chr5:178220089-178220090	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs139642782	chr5:178220116-178220117	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs368335543	chr5:178220134-178220135	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs368084667	chr5:178220168-178220169	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs112277973	chr5:178220174-178220175	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs374654040	chr5:178220178-178220179	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs575029674	chr5:178220179-178220180	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs7733056	chr5:178220184-178220185	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs371761688	chr5:178220186-178220187	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs574239506	chr5:178220205-178220206	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs201674753	chr5:178220206-178220207	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs559649405	chr5:178220211-178220212	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs141397973	chr5:178220241-178220242	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs550664360	chr5:178220246-178220247	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs545458035	chr5:178220250-178220251	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs563752228	chr5:178220323-178220324	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs531050561	chr5:178220327-178220328	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs549168424	chr5:178220352-178220353	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs567360394	chr5:178220356-178220357	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs528341450	chr5:178220373-178220374	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546575204	chr5:178220387-178220388	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs112528353	chr5:178220389-178220390	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs538241429	chr5:178220417-178220418	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs116463518	chr5:178220423-178220424	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs568581708	chr5:178220425-178220426	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535956863	chr5:178220439-178220440	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs555499709	chr5:178220450-178220451	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372465893	chr5:178220465-178220466	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs184150187	chr5:178220489-178220490	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs145768892	chr5:178220524-178220525	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs148868776	chr5:178220525-178220526	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs6600957	chr5:178220548-178220549	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs553379636	chr5:178220563-178220564	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs578221091	chr5:178220565-178220566	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545394506	chr5:178220579-178220580	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2333 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178166600-178224000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr5:178218000-178220400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr5:178218000-178220400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:178218000-178220800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:178220200-178221200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr5:178220400-178221200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr5:178220400-178221200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:178220800-178221200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr5:178221200-178228000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr5:178224000-178224200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
11	chr5:178224000-178224800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr5:178224000-178224800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr5:178226000-178226200	Enhancers	K562	blood
14	chr5:178226200-178230800	Weak transcription	K562	blood
15	chr5:178227200-178232400	Weak transcription	Right Atrium	heart
16	chr5:178228000-178228400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:178228400-178232000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr5:178230800-178231000	ZNF genes & repeats	K562	blood
19	chr5:178230800-178231800	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr5:178230800-178232000	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr5:178231000-178235800	Weak transcription	K562	blood
22	chr5:178232400-178232600	Enhancers	Right Atrium	heart
23	chr5:178235800-178236800	Strong transcription	K562	blood
24	chr5:178236800-178255800	Weak transcription	K562	blood
25	chr5:178241200-178252400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr5:178245200-178245400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr5:178245200-178245600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr5:178251800-178252400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr5:178252200-178253200	Enhancers	H9 Cell Line	embryonic stem cell
30	chr5:178252400-178252600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr5:178252400-178253200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr5:178252400-178253400	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr5:178252400-178254000	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr5:178252400-178254600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr5:178252400-178255000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr5:178252600-178253000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr5:178252600-178253200	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr5:178252600-178254200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr5:178252600-178254400	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr5:178252600-178254400	Enhancers	HMEC	breast
41	chr5:178252600-178254600	Enhancers	NHEK	skin
42	chr5:178252600-178255000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr5:178252800-178253400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr5:178252800-178254000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr5:178252800-178254400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr5:178253000-178253200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr5:178253200-178255800	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr5:178253200-178256000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr5:178253200-178257000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr5:178253200-178257800	Weak transcription	HUES6 Cell Line	embryonic stem cell

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