Variant report

Variant	nsv537248
Chromosome Location	chr4:129658178-129778086
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2738)
CpG islands
(count:1895)
Chromatin interactive
region (count:130)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2738 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:129733069-129733140	K562	blood:	n/a	n/a
2	ARID3A	chr4:129730583-129731709	HepG2	liver:	n/a	chr4:129731284-129731292
3	ARID3A	chr4:129732038-129732519	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:129709063-129709152	K562	blood:	n/a	n/a
5	ARID3A	chr4:129703617-129703832	K562	blood:	n/a	n/a
6	ARID3A	chr4:129752427-129752944	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:129689648-129689845	K562	blood:	n/a	n/a
8	ARID3A	chr4:129730637-129731577	K562	blood:	n/a	chr4:129731284-129731292
9	ARID3A	chr4:129733056-129733419	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:129672594-129672874	K562	blood:	n/a	n/a
11	ATF1	chr4:129692022-129692245	K562	blood:	n/a	n/a
12	ATF2	chr4:129733247-129733506	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr4:129730484-129731078	GM12878	blood:	n/a	n/a
14	ATF2	chr4:129752609-129753033	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr4:129733538-129734069	GM12878	blood:	n/a	n/a
16	ATF2	chr4:129730571-129730942	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr4:129731119-129731494	GM12878	blood:	n/a	n/a
18	ATF2	chr4:129732015-129732582	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr4:129747574-129748193	GM12878	blood:	n/a	n/a
20	ATF2	chr4:129731156-129731606	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr4:129723787-129724248	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr4:129731939-129732672	GM12878	blood:	n/a	n/a
23	ATF2	chr4:129731142-129731783	GM12878	blood:	n/a	n/a
24	ATF2	chr4:129730629-129730989	GM12878	blood:	n/a	n/a
25	ATF2	chr4:129731612-129731877	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr4:129733630-129734051	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr4:129747669-129748111	GM12878	blood:	n/a	n/a
28	ATF2	chr4:129732826-129733531	GM12878	blood:	n/a	n/a
29	ATF2	chr4:129730540-129730947	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr4:129731890-129732722	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr4:129731986-129732799	GM12878	blood:	n/a	n/a
32	ATF3	chr4:129730645-129730969	A549	lung:	n/a	n/a
33	ATF3	chr4:129733184-129733642	K562	blood:	n/a	n/a
34	ATF3	chr4:129733139-129733559	A549	lung:	n/a	chr4:129733161-129733170
35	ATF3	chr4:129658352-129658529	K562	blood:	n/a	n/a
36	ATF3	chr4:129731971-129732548	A549	lung:	n/a	n/a
37	ATF3	chr4:129689614-129689891	K562	blood:	n/a	n/a
38	ATF3	chr4:129733262-129733590	K562	blood:	n/a	n/a
39	ATF3	chr4:129732434-129732753	K562	blood:	n/a	chr4:129732709-129732718
40	ATF3	chr4:129692042-129692244	K562	blood:	n/a	n/a
41	ATF3	chr4:129730573-129731062	A549	lung:	n/a	n/a
42	BACH1	chr4:129752638-129753157	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr4:129744171-129744550	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr4:129732144-129732643	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr4:129732523-129732530	K562	blood:	n/a	n/a
46	BACH1	chr4:129740784-129740831	K562	blood:	n/a	n/a
47	BACH1	chr4:129672639-129672924	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr4:129672535-129672962	K562	blood:	n/a	n/a
49	BACH1	chr4:129723876-129724399	H1-hESC	embryonic stem cell:	n/a	n/a
50	BACH1	chr4:129730606-129731283	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1895 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:129697855-129697905	SAEC	small airway:	n/a
2	chr4:129759716-129759766	K562	blood:	n/a
3	chr4:129731315-129731365	AoSMC	blood vessel:	n/a
4	chr4:129731973-129732023	Caco-2	colon:	n/a
5	chr4:129697855-129697905	SAEC	small airway:	n/a
6	chr4:129759716-129759766	K562	blood:	n/a
7	chr4:129731315-129731365	AoSMC	blood vessel:	n/a
8	chr4:129731973-129732023	Caco-2	colon:	n/a
9	chr4:129733057-129733107	AoSMC	blood vessel:	n/a
10	chr4:129731335-129731385	SK-N-MC	brain:	n/a
11	chr4:129733057-129733107	PFSK-1	brain:	n/a
12	chr4:129732056-129732106	ECC-1	luminal epithelium:	n/a
13	chr4:129730729-129730779	HCF	heart:	n/a
14	chr4:129733571-129733621	SK-N-MC	brain:	n/a
15	chr4:129733887-129733937	HepG2	liver:	n/a
16	chr4:129730137-129730187	GM12891	blood:	n/a
17	chr4:129740752-129740802	BJ	skin:	n/a
18	chr4:129730719-129730769	GM06990	blood:	n/a
19	chr4:129733887-129733937	HRPEpiC	eye:	n/a
20	chr4:129730732-129730782	Jurkat	blood:	n/a
21	chr4:129767588-129767638	A549	lung:	n/a
22	chr4:129732568-129732618	HCF	heart:	n/a
23	chr4:129731315-129731365	HEEpiC	esophagus:	n/a
24	chr4:129730729-129730779	HMEC	breast:	n/a
25	chr4:129730732-129730782	HIPEpiC	eye:	n/a
26	chr4:129747274-129747324	HCPEpiC	choroid plexus:	n/a
27	chr4:129730137-129730187	AG10803	skin:	n/a
28	chr4:129730872-129730922	HL-60	blood:	n/a
29	chr4:129731335-129731385	GM12891	blood:	n/a
30	chr4:129721849-129721899	HNPCEpiC	eye:	n/a
31	chr4:129732568-129732618	GM06990	blood:	n/a
32	chr4:129740752-129740802	NB4	blood:	n/a
33	chr4:129730732-129730782	HRE	kidney:	n/a
34	chr4:129733057-129733107	GM06990	blood:	n/a
35	chr4:129767588-129767638	HRCEpiC	kidney:	n/a
36	chr4:129724002-129724052	PrEC	prostate:	n/a
37	chr4:129733574-129733624	GM19239	blood:	n/a
38	chr4:129740752-129740802	HEK293	kidney:	embryo
39	chr4:129724002-129724052	SK-N-MC	brain:	n/a
40	chr4:129733028-129733078	HAEpiC	amniotic membrane:	n/a
41	chr4:129767588-129767638	NB4	blood:	n/a
42	chr4:129733028-129733078	RPTEC	kidney:	n/a
43	chr4:129731315-129731365	HEK293	kidney:	embryo
44	chr4:129732568-129732618	AoSMC	blood vessel:	n/a
45	chr4:129730872-129730922	SK-N-MC	brain:	n/a
46	chr4:129730732-129730782	MCF-7	breast:	n/a
47	chr4:129732568-129732618	NT2-D1	testis:	n/a
48	chr4:129733571-129733621	PFSK-1	brain:	n/a
49	chr4:129730729-129730779	AG09319	gingival:	n/a
50	chr4:129731315-129731365	SK-N-SH	brain:	n/a

(count:130 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:129730562..129732301-chr4:129775269..129777728,2	K562	blood:
2	chr4:129472659..129478043-chr4:129729703..129733779,4	K562	blood:
3	chr4:129730340..129733748-chr4:130013373..130016609,5	K562	blood:
4	chr4:129736742..129738918-chr4:129767515..129769516,2	K562	blood:
5	chr4:129770197..129772164-chr4:129783210..129785874,2	K562	blood:
6	chr4:129760081..129763027-chr4:129766274..129768354,2	K562	blood:
7	chr4:129731063..129734279-chr4:129754821..129757246,3	K562	blood:
8	chr4:129732800..129733514-chr7:44835890..44836515,2	Hela-S3	cervix:
9	chr4:129730756..129732301-chr4:129776228..129778833,2	K562	blood:
10	chr4:129208294..129210116-chr4:129731375..129734707,3	MCF-7	breast:
11	chr4:129760081..129764752-chr4:129766854..129770363,4	K562	blood:
12	chr4:129725702..129726480-chr4:129789353..129790148,2	MCF-7	breast:
13	chr4:129374782..129377512-chr4:129729521..129732215,3	K562	blood:
14	chr4:129375160..129378617-chr4:129730147..129733611,3	MCF-7	breast:
15	chr4:129473262..129475851-chr4:129658001..129660219,2	K562	blood:
16	chr4:129759776..129761947-chr4:129777321..129779431,2	K562	blood:
17	chr4:129731326..129732115-chr6:26158771..26159658,2	Hela-S3	cervix:
18	chr4:129760491..129763213-chr4:129764575..129766528,2	K562	blood:
19	chr4:129391462..129394361-chr4:129730843..129732581,2	K562	blood:
20	chr4:129702124..129704730-chr4:129730252..129732949,2	K562	blood:
21	chr4:129695090..129697564-chr4:129700193..129701700,2	K562	blood:
22	chr11:62608655..62609419-chr4:129731014..129731869,3	Hela-S3	cervix:
23	chr4:129754977..129757198-chr4:129761484..129764208,2	K562	blood:
24	chr3:61736779..61737344-chr4:129755955..129756840,2	MCF-7	breast:
25	chr4:129658670..129660547-chr4:129733164..129735404,2	K562	blood:
26	chr1:228352349..228353216-chr4:129731096..129731690,2	Hela-S3	cervix:
27	chr4:129691824..129694425-chr4:129696336..129697860,2	K562	blood:
28	chr4:129708061..129710366-chr4:129730711..129732299,2	K562	blood:
29	chr4:129691824..129695688-chr4:129696336..129698007,3	K562	blood:
30	chr4:129732203..129736510-chr4:129738670..129742463,5	MCF-7	breast:
31	chr4:129732985..129735463-chr4:129755056..129756818,2	MCF-7	breast:
32	chr4:129717593..129719726-chr4:129720260..129722513,2	K562	blood:
33	chr4:129730975..129733896-chr4:129754884..129756961,2	MCF-7	breast:
34	chr4:129521730..129523961-chr4:129725803..129727506,2	K562	blood:
35	chr4:129764059..129767011-chr4:129767338..129770023,2	MCF-7	breast:
36	chr4:129730556..129734953-chr4:129772085..129776071,5	K562	blood:
37	chr4:129733589..129734125-chr6:33267187..33267913,2	Hela-S3	cervix:
38	chr4:129762106..129764642-chr4:129772413..129774661,2	K562	blood:
39	chr4:129770901..129772590-chr4:129787099..129788677,2	K562	blood:
40	chr4:129518963..129527383-chr4:129727996..129735335,14	K562	blood:
41	chr4:129732385..129733951-chr4:129746938..129749737,2	MCF-7	breast:
42	chr4:129730688..129731418-chr6:24720530..24721134,2	Hela-S3	cervix:
43	chr4:129686945..129689480-chr4:129691939..129694089,3	K562	blood:
44	chr4:129731044..129733877-chr4:129757449..129759486,2	MCF-7	breast:
45	chr4:129691824..129694425-chr4:129696336..129697860,2	K562	blood:
46	chr4:129732370..129733941-chr4:129735604..129737176,2	MCF-7	breast:
47	chr4:129206178..129209105-chr4:129728853..129732712,4	K562	blood:
48	chr4:129728325..129729008-chr8:43092928..43093431,2	MCF-7	breast:
49	chr4:129695090..129697564-chr4:129700193..129701700,2	K562	blood:
50	chr4:100869660..100871292-chr4:129732222..129733752,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHF17-5	chr4:129676666-129676819	NONHSAT098278
2	lnc-PHF17-2	chr4:129659361-129660069	l_2730_chr4:129656347-129659963_placenta
3	lnc-PHF17-5	chr4:129677040-129677278	NONHSAT098278
4	lnc-SCLT1-5	chr4:129708577-129709892	ucscGeneNc_uc003igi_1
5	lnc-SCLT1-5	chr4:129710830-129711049	ucscGeneNc_uc003igi_1
6	lnc-PHF17-5	chr4:129678040-129678156	NONHSAT098278
7	lnc-PHF17-5	chr4:129696672-129697105	NONHSAT098278

No data

Variant related genes	Relation type
ENSG00000238802	TF binding region
JADE1	TF binding region
ENSG00000238802	CpG island
JADE1	CpG island
ENSG00000230648	chromatin interactions
ENSG00000148773	chromatin interactions
ENSG00000196262	chromatin interactions
ENSG00000164040	chromatin interactions
ENSG00000251432	chromatin interactions
ENSG00000103126	chromatin interactions
ENSG00000164109	chromatin interactions
ENSG00000151466	chromatin interactions
ENSG00000175854	chromatin interactions
ENSG00000138709	chromatin interactions
ENSG00000248187	chromatin interactions
ENSG00000273077	chromatin interactions
ENSG00000123124	chromatin interactions
ENSG00000112308	chromatin interactions
ENSG00000204344	chromatin interactions
ENSG00000145050	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000204348	chromatin interactions
ENSG00000250938	chromatin interactions
ENSG00000203684	chromatin interactions
ENSG00000248802	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000112739	chromatin interactions
ENSG00000167110	chromatin interactions
ENSG00000077684	chromatin interactions
ENSG00000151470	chromatin interactions
ENSG00000245322	chromatin interactions

Extended variants
information (count: 4672 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:4672 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74534982	chr4:129658194-129658195	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs10006675	chr4:129658198-129658199	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs527795503	chr4:129658226-129658227	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs115866522	chr4:129658241-129658242	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs79713333	chr4:129658253-129658254	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs537157889	chr4:129658258-129658259	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs183923315	chr4:129658326-129658327	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs138663995	chr4:129658338-129658339	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs573787763	chr4:129658398-129658399	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs553734052	chr4:129658417-129658418	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs578254583	chr4:129658425-129658426	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs561173831	chr4:129658443-129658444	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs141202876	chr4:129658444-129658445	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs72918412	chr4:129658454-129658455	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs79749039	chr4:129658476-129658477	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs530298287	chr4:129658522-129658523	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs138865823	chr4:129658619-129658620	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs540121241	chr4:129658649-129658650	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs564808843	chr4:129658653-129658654	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs550247075	chr4:129658657-129658658	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs373724189	chr4:129658659-129658660	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs115835792	chr4:129658660-129658661	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs531029604	chr4:129658690-129658691	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs371849626	chr4:129658716-129658717	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs142045502	chr4:129658719-129658720	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs534985542	chr4:129658724-129658725	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs13115151	chr4:129658732-129658733	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs552157719	chr4:129658733-129658734	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs375715587	chr4:129658736-129658737	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs34150232	chr4:129658755-129658756	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs567776304	chr4:129658770-129658771	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs144765874	chr4:129658774-129658775	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs76441501	chr4:129658816-129658817	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs569397763	chr4:129658838-129658839	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs114369530	chr4:129658876-129658877	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs188666777	chr4:129658899-129658900	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs35708180	chr4:129658909-129658910	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs181722064	chr4:129658956-129658957	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs148145058	chr4:129658992-129658993	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs558138054	chr4:129658998-129658999	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs576716061	chr4:129659059-129659060	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs116510239	chr4:129659105-129659106	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs187146198	chr4:129659162-129659163	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs529880140	chr4:129659196-129659197	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs141990762	chr4:129659210-129659211	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs191628633	chr4:129659230-129659231	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs574721753	chr4:129659250-129659251	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182265919	chr4:129659253-129659254	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs528602936	chr4:129659261-129659262	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs187235692	chr4:129659286-129659287	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Developmental delay	21147756	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3048 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:129633000-129689600	Weak transcription	Right Atrium	heart
2	chr4:129647000-129658200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr4:129653800-129658200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr4:129654000-129658200	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr4:129654000-129658400	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr4:129654200-129658200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr4:129654600-129658400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr4:129654800-129658200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr4:129658000-129658600	Enhancers	H1 Cell Line	embryonic stem cell
10	chr4:129658000-129659000	Enhancers	Fetal Heart	heart
11	chr4:129658200-129658600	Enhancers	H9 Cell Line	embryonic stem cell
12	chr4:129658200-129658800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr4:129658200-129658800	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr4:129658200-129658800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr4:129658200-129658800	Enhancers	K562	blood
16	chr4:129658400-129658600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:129658400-129658800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:129658400-129658800	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr4:129658400-129658800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr4:129658400-129658800	Enhancers	Left Ventricle	heart
21	chr4:129658600-129659800	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr4:129658600-129660000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr4:129658600-129663200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr4:129658800-129660600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr4:129658800-129661800	Weak transcription	Left Ventricle	heart
26	chr4:129659800-129660000	Enhancers	H1 Cell Line	embryonic stem cell
27	chr4:129660400-129660600	Enhancers	H9 Cell Line	embryonic stem cell
28	chr4:129660400-129660600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr4:129660600-129660800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr4:129661200-129662000	Enhancers	Muscle Satellite Cultured Cells	--
31	chr4:129663200-129663400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr4:129663400-129672200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr4:129666400-129666600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr4:129666600-129692400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr4:129666800-129679000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr4:129672200-129672400	Enhancers	K562	blood
37	chr4:129672200-129672800	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr4:129672200-129673000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr4:129672400-129673000	Flanking Active TSS	K562	blood
40	chr4:129672800-129674600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr4:129673000-129673200	Enhancers	K562	blood
42	chr4:129673000-129678800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr4:129674600-129674800	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr4:129674600-129675600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr4:129674600-129679000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr4:129675000-129675400	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr4:129675600-129678800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr4:129678600-129679200	Enhancers	A549	lung
49	chr4:129678600-129679800	Enhancers	Fetal Heart	heart
50	chr4:129678800-129679200	Enhancers	H9 Cell Line	embryonic stem cell

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