Variant report

Variant	nsv883008
Chromosome Location	chr5:145509728-145642925
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2259)
CpG islands
(count:1221)
Chromatin interactive
region (count:116)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2259 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:145592962-145593348	K562	blood:	n/a	n/a
2	ARID3A	chr5:145516863-145516977	K562	blood:	n/a	n/a
3	ARID3A	chr5:145582474-145583196	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:145593038-145593693	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:145548626-145549020	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:145517540-145518017	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:145561812-145562714	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:145572277-145572484	K562	blood:	n/a	n/a
9	ARID3A	chr5:145570492-145570635	HepG2	liver:	n/a	n/a
10	ARID3A	chr5:145582257-145583366	K562	blood:	n/a	n/a
11	ARID3A	chr5:145561689-145562556	K562	blood:	n/a	n/a
12	ATF1	chr5:145582723-145583251	K562	blood:	n/a	n/a
13	ATF1	chr5:145572359-145572575	K562	blood:	n/a	n/a
14	ATF1	chr5:145561969-145562643	K562	blood:	n/a	n/a
15	ATF1	chr5:145510077-145510250	K562	blood:	n/a	n/a
16	ATF1	chr5:145551256-145551280	K562	blood:	n/a	n/a
17	ATF2	chr5:145582497-145583292	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr5:145582523-145583339	GM12878	blood:	n/a	n/a
19	ATF2	chr5:145561863-145562720	GM12878	blood:	n/a	chr5:145562365-145562376
20	ATF2	chr5:145561804-145562616	GM12878	blood:	n/a	chr5:145562365-145562376
21	ATF2	chr5:145585728-145586264	GM12878	blood:	n/a	n/a
22	ATF2	chr5:145561795-145562742	H1-hESC	embryonic stem cell:	n/a	chr5:145562365-145562376
23	ATF2	chr5:145553057-145553609	GM12878	blood:	n/a	n/a
24	ATF2	chr5:145561959-145562657	H1-hESC	embryonic stem cell:	n/a	chr5:145562365-145562376
25	ATF3	chr5:145562029-145562500	K562	blood:	n/a	chr5:145562364-145562375 chr5:145562363-145562376 chr5:145562366-145562377 chr5:145562367-145562377 chr5:145562367-145562374 chr5:145562365-145562378 chr5:145562366-145562374 chr5:145562363-145562378 chr5:145562364-145562374 chr5:145562367-145562375 chr5:145562355-145562375
26	ATF3	chr5:145517501-145517708	HepG2	liver:	n/a	n/a
27	ATF3	chr5:145572119-145572521	K562	blood:	n/a	n/a
28	ATF3	chr5:145582548-145583298	A549	lung:	n/a	chr5:145582838-145582846
29	ATF3	chr5:145572846-145573233	K562	blood:	n/a	n/a
30	ATF3	chr5:145561998-145562564	A549	lung:	n/a	chr5:145562364-145562375 chr5:145562363-145562376 chr5:145562366-145562377 chr5:145562367-145562377 chr5:145562367-145562374 chr5:145562365-145562378 chr5:145562366-145562374 chr5:145562363-145562378 chr5:145562364-145562374 chr5:145562367-145562375 chr5:145562355-145562375
31	ATF3	chr5:145581363-145581609	K562	blood:	n/a	n/a
32	ATF3	chr5:145561794-145562750	A549	lung:	n/a	chr5:145562364-145562375 chr5:145562363-145562376 chr5:145562366-145562377 chr5:145562367-145562377 chr5:145562367-145562374 chr5:145562365-145562378 chr5:145562366-145562374 chr5:145562363-145562378 chr5:145562364-145562374 chr5:145562367-145562375 chr5:145562355-145562375
33	ATF3	chr5:145561978-145562457	H1-hESC	embryonic stem cell:	n/a	chr5:145562364-145562375 chr5:145562363-145562376 chr5:145562366-145562377 chr5:145562367-145562377 chr5:145562367-145562374 chr5:145562365-145562378 chr5:145562366-145562374 chr5:145562363-145562378 chr5:145562364-145562374 chr5:145562367-145562375 chr5:145562355-145562375
34	ATF3	chr5:145561913-145562552	K562	blood:	n/a	chr5:145562364-145562375 chr5:145562363-145562376 chr5:145562366-145562377 chr5:145562367-145562377 chr5:145562367-145562374 chr5:145562365-145562378 chr5:145562366-145562374 chr5:145562363-145562378 chr5:145562364-145562374 chr5:145562367-145562375 chr5:145562355-145562375
35	BACH1	chr5:145561812-145562672	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr5:145582680-145583388	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr5:145582529-145582857	K562	blood:	n/a	n/a
38	BACH1	chr5:145620815-145620864	K562	blood:	n/a	n/a
39	BATF	chr5:145582607-145582889	GM12878	blood:	n/a	chr5:145582770-145582780
40	BATF	chr5:145582596-145583207	GM12878	blood:	n/a	chr5:145582770-145582780
41	BATF	chr5:145618600-145618803	GM12878	blood:	n/a	chr5:145618713-145618724
42	BATF	chr5:145562035-145562498	GM12878	blood:	n/a	n/a
43	BATF	chr5:145562820-145563124	GM12878	blood:	n/a	n/a
44	BATF	chr5:145562738-145563155	GM12878	blood:	n/a	n/a
45	BCL11A	chr5:145553130-145553474	GM12878	blood:	n/a	n/a
46	BCL3	chr5:145561846-145562716	A549	lung:	n/a	n/a
47	BCL3	chr5:145561680-145562656	A549	lung:	n/a	n/a
48	BCL3	chr5:145582511-145582937	GM12878	blood:	n/a	chr5:145582769-145582778 chr5:145582882-145582895 chr5:145582885-145582898
49	BCLAF1	chr5:145561912-145562656	GM12878	blood:	n/a	n/a
50	BCLAF1	chr5:145553066-145553628	GM12878	blood:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:145587156-145587206	HL-60	blood:	n/a
2	chr5:145587156-145587206	HL-60	blood:	n/a
3	chr5:145583220-145583270	ProgFib	skin:	n/a
4	chr5:145587156-145587206	HEEpiC	esophagus:	n/a
5	chr5:145562268-145562318	K562	blood:	n/a
6	chr5:145562699-145562749	A549	lung:	n/a
7	chr5:145583220-145583270	GM12892	blood:	n/a
8	chr5:145562428-145562478	Caco-2	colon:	n/a
9	chr5:145582897-145582947	HCF	heart:	n/a
10	chr5:145562426-145562476	PFSK-1	brain:	n/a
11	chr5:145562530-145562580	IMR90	lung:	fetal
12	chr5:145579573-145579623	GM06990	blood:	n/a
13	chr5:145583122-145583172	NB4	blood:	n/a
14	chr5:145562478-145562528	HNPCEpiC	eye:	n/a
15	chr5:145562434-145562484	GM19239	blood:	n/a
16	chr5:145582568-145582618	HCF	heart:	n/a
17	chr5:145587156-145587206	A549	lung:	n/a
18	chr5:145562699-145562749	HRCEpiC	kidney:	n/a
19	chr5:145579573-145579623	SKMC	muscle:	n/a
20	chr5:145562434-145562484	HEK293	kidney:	embryo
21	chr5:145583122-145583172	AG09319	gingival:	n/a
22	chr5:145583025-145583075	PFSK-1	brain:	n/a
23	chr5:145562428-145562478	BJ	skin:	n/a
24	chr5:145582897-145582947	A549	lung:	n/a
25	chr5:145583671-145583721	Jurkat	blood:	n/a
26	chr5:145583671-145583721	SK-N-SH	brain:	n/a
27	chr5:145562428-145562478	ovcar-3	ovarian:	n/a
28	chr5:145583220-145583270	HEEpiC	esophagus:	n/a
29	chr5:145579573-145579623	PANC-1	pancreas:	n/a
30	chr5:145562478-145562528	LNCaP	prostate:	n/a
31	chr5:145562370-145562420	HRPEpiC	eye:	n/a
32	chr5:145587156-145587206	HCF	heart:	n/a
33	chr5:145587156-145587206	AG09319	gingival:	n/a
34	chr5:145562478-145562528	SK-N-SH	brain:	n/a
35	chr5:145582897-145582947	GM12892	blood:	n/a
36	chr5:145562530-145562580	BJ	skin:	n/a
37	chr5:145583122-145583172	GM19239	blood:	n/a
38	chr5:145582568-145582618	RPTEC	kidney:	n/a
39	chr5:145583510-145583560	HCT-116	colon:	n/a
40	chr5:145562268-145562318	GM12891	blood:	n/a
41	chr5:145562370-145562420	HCPEpiC	choroid plexus:	n/a
42	chr5:145562426-145562476	HEEpiC	esophagus:	n/a
43	chr5:145583510-145583560	AG04450	lung:	fetal
44	chr5:145562530-145562580	PANC-1	pancreas:	n/a
45	chr5:145562434-145562484	HCPEpiC	choroid plexus:	n/a
46	chr5:145583671-145583721	BE2_C	brain:	n/a
47	chr5:145587156-145587206	BE2_C	brain:	n/a
48	chr5:145583025-145583075	AG04449	skin:	fetal
49	chr5:145562434-145562484	HL-60	blood:	n/a
50	chr5:145583408-145583458	SKMC	muscle:	n/a

(count:116 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:145525794..145527740-chr5:145551579..145553885,3	K562	blood:
2	chr5:145559635..145563527-chr5:145825770..145828320,3	K562	blood:
3	chr5:145557742..145559707-chr5:145585614..145588262,3	K562	blood:
4	chr5:145612339..145614307-chr5:145615895..145618813,2	MCF-7	breast:
5	chr5:145540004..145542261-chr5:145544154..145547069,3	K562	blood:
6	chr5:145557742..145559707-chr5:145585614..145588262,3	K562	blood:
7	chr5:145543973..145545500-chr5:145559065..145562026,2	K562	blood:
8	chr5:145560642..145563806-chr5:145566350..145569083,3	MCF-7	breast:
9	chr5:145567639..145569805-chr5:145575511..145577560,2	K562	blood:
10	chr5:145573844..145575489-chr5:145577748..145580152,2	K562	blood:
11	chr5:145625814..145628687-chr5:145636719..145638380,2	K562	blood:
12	chr5:145540004..145542261-chr5:145544154..145547069,3	K562	blood:
13	chr5:145556363..145559212-chr5:145560408..145562154,3	K562	blood:
14	chr5:145543670..145545508-chr5:145560602..145562850,2	MCF-7	breast:
15	chr5:145544700..145547234-chr5:145551344..145553851,2	K562	blood:
16	chr5:145625869..145628007-chr5:145631607..145633546,2	K562	blood:
17	chr5:145555213..145560576-chr5:145560598..145562206,4	K562	blood:
18	chr5:145573844..145576885-chr5:145577748..145580180,3	K562	blood:
19	chr5:145507255..145510275-chr5:145511720..145513708,3	K562	blood:
20	chr5:145594426..145596514-chr5:145599170..145601456,2	K562	blood:
21	chr5:145536432..145538417-chr5:145545755..145548340,2	K562	blood:
22	chr5:145581405..145584024-chr5:145596123..145597883,2	K562	blood:
23	chr5:145595165..145597126-chr5:145598903..145601685,2	K562	blood:
24	chr19:49496287..49496957-chr5:145561885..145562408,2	HCT-116	colon:
25	chr5:145551306..145553774-chr5:145557195..145559625,2	K562	blood:
26	chr5:145559745..145561849-chr5:145588233..145589890,2	K562	blood:
27	chr5:145570785..145572816-chr5:145582211..145584363,2	MCF-7	breast:
28	chr5:145582359..145584728-chr5:145597576..145599110,2	MCF-7	breast:
29	chr5:145625869..145628007-chr5:145631607..145633546,2	K562	blood:
30	chr5:145573844..145575489-chr5:145577748..145580152,2	K562	blood:
31	chr5:145544700..145547234-chr5:145551344..145553851,2	K562	blood:
32	chr5:145549719..145552981-chr5:145557063..145560291,4	MCF-7	breast:
33	chr5:145417177..145419774-chr5:145514688..145516559,2	K562	blood:
34	chr5:145531283..145533284-chr5:145537257..145540208,2	K562	blood:
35	chr5:145562850..145566563-chr5:145571128..145574037,3	MCF-7	breast:
36	chr5:145560893..145564215-chr5:145581108..145584712,3	MCF-7	breast:
37	chr5:145596117..145598265-chr5:145605012..145606909,2	K562	blood:
38	chr5:145547972..145550072-chr5:145559815..145562335,2	K562	blood:
39	chr5:145612339..145614307-chr5:145615895..145618813,2	MCF-7	breast:
40	chr5:145536432..145538417-chr5:145545755..145548340,2	K562	blood:
41	chr5:145591065..145593762-chr5:145596165..145598951,2	K562	blood:
42	chr5:145577261..145580172-chr5:145580674..145584056,4	K562	blood:
43	chr5:145588075..145590940-chr5:145591754..145595862,4	K562	blood:
44	chr5:145560592..145565120-chr5:145580444..145584486,7	K562	blood:
45	chr5:145551516..145553977-chr5:145559737..145562085,2	K562	blood:
46	chr5:145560704..145564062-chr5:145572842..145575538,3	K562	blood:
47	chr5:145564948..145567866-chr5:145592052..145594140,2	K562	blood:
48	chr5:145582693..145585612-chr5:145586430..145590293,7	MCF-7	breast:
49	chr5:145507255..145510275-chr5:145511720..145513708,3	K562	blood:
50	chr5:145607480..145610119-chr5:145611867..145613573,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH3RF2-5	chr5:145518334-145518571	NONHSAT104396
2	lnc-SH3RF2-4	chr5:145517318-145517401	NONHSAT104395
3	lnc-SH3RF2-4	chr5:145517708-145517944	NONHSAT104395

No data

Variant related genes	Relation type
LARS	TF binding region
RBM27	TF binding region
RNU7-180P	TF binding region
ENSG00000239602	TF binding region
ENSG00000239317	TF binding region
LARS	CpG island
RBM27	CpG island
RNU7-180P	CpG island
ENSG00000239602	CpG island
ENSG00000239317	CpG island
ENSG00000113649	chromatin interactions
ENSG00000196562	chromatin interactions
ENSG00000091009	chromatin interactions
ENSG00000133706	chromatin interactions
ENSG00000165804	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000104812	chromatin interactions
ENSG00000183207	chromatin interactions
ENSG00000232070	chromatin interactions

Extended variants
information (count: 5232 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:5232 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17104268	chr5:145509728-145509729	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548773989	chr5:145509760-145509761	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs373799044	chr5:145509814-145509815	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs530434307	chr5:145509830-145509831	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs549899494	chr5:145509839-145509840	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs570080802	chr5:145509848-145509849	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs191151724	chr5:145509851-145509852	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs182471010	chr5:145509910-145509911	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs565853116	chr5:145509936-145509937	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs146148101	chr5:145509965-145509966	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs554345551	chr5:145509991-145509992	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs574602822	chr5:145509998-145509999	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs537390201	chr5:145510050-145510051	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs34794547	chr5:145510123-145510124	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs576797534	chr5:145510128-145510129	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs545896994	chr5:145510129-145510130	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs36098188	chr5:145510143-145510144	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs572980257	chr5:145510154-145510155	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs148804357	chr5:145510175-145510176	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs17427691	chr5:145510176-145510177	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs530326475	chr5:145510197-145510198	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs377234343	chr5:145510202-145510203	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs188461024	chr5:145510240-145510241	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs1911112	chr5:145510261-145510262	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs1911113	chr5:145510277-145510278	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs552175760	chr5:145510314-145510315	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs114406964	chr5:145510363-145510364	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs115245364	chr5:145510408-145510409	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs547971312	chr5:145510438-145510439	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs561654902	chr5:145510439-145510440	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs568291106	chr5:145510487-145510488	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs536922967	chr5:145510521-145510522	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs372064359	chr5:145510534-145510535	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs142402814	chr5:145510538-145510539	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs375047028	chr5:145510542-145510543	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs369382242	chr5:145510554-145510555	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs200080099	chr5:145510562-145510563	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs375151931	chr5:145510578-145510579	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs141234474	chr5:145510605-145510606	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs150185886	chr5:145510624-145510625	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs539395367	chr5:145510666-145510667	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs369569573	chr5:145510684-145510685	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs553015995	chr5:145510688-145510689	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs572968230	chr5:145510694-145510695	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs541995005	chr5:145510695-145510696	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs371690781	chr5:145510697-145510698	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs561303719	chr5:145510702-145510703	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs368403612	chr5:145510722-145510723	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs191652332	chr5:145510728-145510729	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs182397943	chr5:145510776-145510777	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	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
Breast cancer	21858162	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
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	16864856	CNVD
small cell lung cancer	20016488	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
Acute lymphoblastic leukemia	21339820	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	20864512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3971 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:145481200-145560200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:145490800-145535200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:145491000-145509800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr5:145491000-145510600	Strong transcription	HSMM	muscle
5	chr5:145491000-145517600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr5:145491000-145518800	Strong transcription	Dnd41	blood
7	chr5:145491000-145542200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:145491000-145551600	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr5:145491000-145553800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:145491000-145560200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr5:145491200-145509800	Strong transcription	Fetal Muscle Trunk	muscle
12	chr5:145491200-145518000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr5:145491200-145534000	Strong transcription	Osteobl	bone
14	chr5:145491200-145552600	Strong transcription	Primary monocytes fromperipheralblood	blood
15	chr5:145491200-145560200	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr5:145491200-145560200	Strong transcription	HUES6 Cell Line	embryonic stem cell
17	chr5:145491200-145560800	Weak transcription	Stomach Mucosa	stomach
18	chr5:145491400-145510000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr5:145491400-145512400	Weak transcription	Right Ventricle	heart
20	chr5:145491400-145515400	Strong transcription	Liver	Liver
21	chr5:145491400-145516200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr5:145491400-145516600	Strong transcription	NH-A	brain
23	chr5:145491400-145560000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr5:145491400-145560400	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr5:145491600-145509800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr5:145491600-145557000	Strong transcription	Primary T helper cells fromperipheralblood	blood
27	chr5:145491600-145559800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
28	chr5:145491800-145515400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr5:145491800-145524800	Strong transcription	Primary T cells fromperipheralblood	blood
30	chr5:145491800-145541400	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr5:145491800-145546400	Strong transcription	H1 Cell Line	embryonic stem cell
32	chr5:145492000-145552200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr5:145492200-145510000	Strong transcription	Duodenum Mucosa	Duodenum
34	chr5:145492200-145560200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
35	chr5:145494000-145520000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr5:145494600-145511200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr5:145494600-145511200	Weak transcription	Fetal Intestine Small	intestine
38	chr5:145494600-145513400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr5:145495200-145515600	Strong transcription	Primary B cells from cord blood	blood
40	chr5:145495400-145509800	Strong transcription	Rectal Mucosa Donor 29	rectum
41	chr5:145495400-145517000	Strong transcription	A549	lung
42	chr5:145495400-145517800	Strong transcription	Primary T helper cells PMA-I stimulated	--
43	chr5:145495800-145519400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr5:145495800-145559200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr5:145496000-145514800	Strong transcription	Rectal Mucosa Donor 31	rectum
46	chr5:145496200-145552200	Strong transcription	Primary B cells from peripheral blood	blood
47	chr5:145497000-145515800	Strong transcription	Fetal Intestine Large	intestine
48	chr5:145497200-145513000	Strong transcription	Hela-S3	cervix
49	chr5:145497200-145517600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr5:145497600-145516000	Strong transcription	K562	blood

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