Variant report

Variant	esv2763866
Chromosome Location	chr5:112254282-112284223
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1236)
CpG islands
(count:674)
Chromatin interactive
region (count:39)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1236 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:112258093-112258188	K562	blood:	n/a	n/a
2	ARID3A	chr5:112267194-112267535	K562	blood:	n/a	n/a
3	ARID3A	chr5:112257795-112258246	HepG2	liver:	n/a	n/a
4	ATF1	chr5:112267212-112267596	K562	blood:	n/a	n/a
5	ATF2	chr5:112264965-112266095	GM12878	blood:	n/a	n/a
6	ATF2	chr5:112265599-112265981	GM12878	blood:	n/a	n/a
7	ATF2	chr5:112258946-112259878	GM12878	blood:	n/a	n/a
8	ATF2	chr5:112257713-112258314	GM12878	blood:	n/a	n/a
9	BACH1	chr5:112258052-112258220	K562	blood:	n/a	n/a
10	BACH1	chr5:112256546-112256759	K562	blood:	n/a	n/a
11	BACH1	chr5:112256913-112258344	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr5:112265623-112266012	GM12878	blood:	n/a	n/a
13	BATF	chr5:112265670-112265971	GM12878	blood:	n/a	n/a
14	BATF	chr5:112259313-112259635	GM12878	blood:	n/a	n/a
15	BATF	chr5:112264992-112265507	GM12878	blood:	n/a	n/a
16	BATF	chr5:112265073-112265384	GM12878	blood:	n/a	n/a
17	BCL11A	chr5:112265622-112265956	GM12878	blood:	n/a	n/a
18	BCL11A	chr5:112265065-112265372	GM12878	blood:	n/a	n/a
19	BCL11A	chr5:112265585-112265966	GM12878	blood:	n/a	n/a
20	BCL11A	chr5:112265009-112265487	GM12878	blood:	n/a	n/a
21	BCL3	chr5:112257489-112258309	A549	lung:	n/a	chr5:112257949-112257958 chr5:112257544-112257557
22	BCLAF1	chr5:112257656-112258408	GM12878	blood:	n/a	chr5:112257949-112257958
23	BCLAF1	chr5:112256742-112257252	GM12878	blood:	n/a	chr5:112256800-112256813
24	BCLAF1	chr5:112264948-112265376	GM12878	blood:	n/a	n/a
25	BCLAF1	chr5:112257645-112258320	GM12878	blood:	n/a	chr5:112257949-112257958
26	BCLAF1	chr5:112265580-112266068	GM12878	blood:	n/a	n/a
27	BCLAF1	chr5:112259019-112260080	GM12878	blood:	n/a	n/a
28	BHLHE40	chr5:112256720-112258353	K562	blood:	n/a	chr5:112257532-112257548 chr5:112257958-112257974 chr5:112257707-112257723 chr5:112257717-112257733 chr5:112257538-112257554
29	BHLHE40	chr5:112256719-112257438	GM12878	blood:	n/a	n/a
30	BHLHE40	chr5:112257784-112258307	GM12878	blood:	n/a	chr5:112257958-112257974
31	BHLHE40	chr5:112267159-112267573	K562	blood:	n/a	n/a
32	BRCA1	chr5:112256818-112257173	GM12878	blood:	n/a	n/a
33	BRCA1	chr5:112256576-112257325	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr5:112257834-112258148	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr5:112257073-112257106	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr5:112257793-112258130	GM12878	blood:	n/a	n/a
37	BRCA1	chr5:112258120-112258145	H1-hESC	embryonic stem cell:	n/a	n/a
38	CBX3	chr5:112257677-112258361	K562	blood:	n/a	n/a
39	CBX3	chr5:112267158-112267592	K562	blood:	n/a	n/a
40	CCNT2	chr5:112256877-112258378	K562	blood:	n/a	n/a
41	CCNT2	chr5:112267127-112267515	K562	blood:	n/a	n/a
42	CEBPB	chr5:112263437-112263707	MCF-7	breast:	n/a	n/a
43	CEBPB	chr5:112269255-112269635	Hela-S3	cervix:	n/a	chr5:112269401-112269412 chr5:112269407-112269418
44	CEBPB	chr5:112264808-112265008	K562	blood:	n/a	n/a
45	CEBPB	chr5:112258060-112258195	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr5:112257756-112258249	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr5:112263479-112263676	HepG2	liver:	n/a	n/a
48	CEBPB	chr5:112258026-112258171	HepG2	liver:	n/a	n/a
49	CEBPB	chr5:112263515-112263665	A549	lung:	n/a	n/a
50	CEBPB	chr5:112256650-112257368	Hela-S3	cervix:	n/a	n/a

(count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:112258268-112258318	GM19239	blood:	n/a
2	chr5:112257968-112258018	SKMC	muscle:	n/a
3	chr5:112256918-112256968	H1-hESC	embryonic stem cell:	embryo
4	chr5:112258268-112258318	GM19239	blood:	n/a
5	chr5:112257968-112258018	SKMC	muscle:	n/a
6	chr5:112256918-112256968	H1-hESC	embryonic stem cell:	embryo
7	chr5:112257975-112258025	PFSK-1	brain:	n/a
8	chr5:112258268-112258318	U87	brain:	n/a
9	chr5:112258299-112258349	GM06990	blood:	n/a
10	chr5:112258649-112258699	Hepatocyte	liver:	n/a
11	chr5:112256918-112256968	GM06990	blood:	n/a
12	chr5:112256918-112256968	RPTEC	kidney:	n/a
13	chr5:112257612-112257662	NB4	blood:	n/a
14	chr5:112258374-112258424	AG09309	skin:	n/a
15	chr5:112257612-112257662	PFSK-1	brain:	n/a
16	chr5:112258131-112258181	CMK	blood:	n/a
17	chr5:112257975-112258025	SK-N-MC	brain:	n/a
18	chr5:112258299-112258349	HCF	heart:	n/a
19	chr5:112257968-112258018	HepG2	liver:	n/a
20	chr5:112258131-112258181	ovcar-3	ovarian:	n/a
21	chr5:112257968-112258018	HIPEpiC	eye:	n/a
22	chr5:112258268-112258318	NH-A	brain:	n/a
23	chr5:112257968-112258018	ECC-1	luminal epithelium:	n/a
24	chr5:112258131-112258181	HCF	heart:	n/a
25	chr5:112258299-112258349	AG09319	gingival:	n/a
26	chr5:112258299-112258349	BE2_C	brain:	n/a
27	chr5:112257116-112257166	PFSK-1	brain:	n/a
28	chr5:112258126-112258176	Hepatocyte	liver:	n/a
29	chr5:112258126-112258176	BE2_C	brain:	n/a
30	chr5:112258268-112258318	NHBE	bronchial:	n/a
31	chr5:112257116-112257166	HRPEpiC	eye:	n/a
32	chr5:112258374-112258424	Hepatocyte	liver:	n/a
33	chr5:112256918-112256968	HL-60	blood:	n/a
34	chr5:112257612-112257662	PANC-1	pancreas:	n/a
35	chr5:112258649-112258699	HMEC	breast:	n/a
36	chr5:112257116-112257166	HEEpiC	esophagus:	n/a
37	chr5:112258268-112258318	SK-N-SH	brain:	n/a
38	chr5:112258374-112258424	GM12878	blood:	n/a
39	chr5:112258268-112258318	GM12878	blood:	n/a
40	chr5:112258268-112258318	PANC-1	pancreas:	n/a
41	chr5:112258126-112258176	NT2-D1	testis:	n/a
42	chr5:112258374-112258424	HRE	kidney:	n/a
43	chr5:112257612-112257662	NT2-D1	testis:	n/a
44	chr5:112258649-112258699	Caco-2	colon:	n/a
45	chr5:112258299-112258349	NHBE	bronchial:	n/a
46	chr5:112256918-112256968	AG04450	lung:	fetal
47	chr5:112257975-112258025	AG09309	skin:	n/a
48	chr5:112258131-112258181	HEK293	kidney:	embryo
49	chr5:112258299-112258349	HMEC	breast:	n/a
50	chr5:112258299-112258349	HNPCEpiC	eye:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:112263017..112264947-chr5:112304699..112307617,2	MCF-7	breast:
2	chr5:112253073..112255997-chr5:112284078..112285645,2	K562	blood:
3	chr5:112256656..112258346-chr5:112281067..112283424,2	MCF-7	breast:
4	chr16:81069322..81070029-chr5:112256640..112257405,2	Hela-S3	cervix:
5	chr5:112243328..112246108-chr5:112252960..112255177,2	MCF-7	breast:
6	chr5:112255746..112257849-chr5:112312359..112314246,3	MCF-7	breast:
7	chr5:112252495..112254832-chr5:112301145..112303115,2	K562	blood:
8	chr5:112252458..112254818-chr5:112292295..112294312,2	K562	blood:
9	chr5:112223765..112227904-chr5:112256681..112259724,3	K562	blood:
10	chr5:112201095..112203323-chr5:112277431..112279323,2	K562	blood:
11	chr5:112255209..112259355-chr5:112310614..112316433,9	K562	blood:
12	chr5:112254440..112257035-chr5:112267383..112269669,3	K562	blood:
13	chr5:112197244..112199299-chr5:112253237..112254952,2	K562	blood:
14	chr5:112262263..112263764-chr5:112265083..112267354,2	K562	blood:
15	chr5:112256150..112258006-chr5:112282214..112285129,2	K562	blood:
16	chr5:112132025..112134986-chr5:112254619..112257174,2	K562	blood:
17	chr5:112258754..112260468-chr5:112260829..112262760,2	MCF-7	breast:
18	chr5:112253344..112255730-chr5:112269581..112271953,2	MCF-7	breast:
19	chr5:112257953..112260534-chr5:112261004..112262710,2	K562	blood:
20	chr5:112252465..112254297-chr5:112272394..112274579,2	K562	blood:
21	chr5:112195239..112200315-chr5:112255126..112261929,8	MCF-7	breast:
22	chr5:112255808..112259712-chr5:112262639..112265626,6	MCF-7	breast:
23	chr5:112255914..112262078-chr5:112308752..112315375,16	MCF-7	breast:
24	chr5:112254019..112256413-chr5:112263500..112265377,2	MCF-7	breast:
25	chr5:112258023..112259796-chr5:112264291..112266888,2	K562	blood:
26	chr5:112254019..112256413-chr5:112263500..112265377,2	MCF-7	breast:
27	chr5:111496112..111498947-chr5:112256676..112259616,2	K562	blood:
28	chr5:112196983..112197664-chr5:112257709..112258331,2	Hela-S3	cervix:
29	chr5:112253961..112259306-chr5:112310933..112315767,8	K562	blood:
30	chr5:112258754..112260468-chr5:112260829..112262760,2	MCF-7	breast:
31	chr5:112254440..112257035-chr5:112267383..112269669,3	K562	blood:
32	chr5:112030572..112032365-chr5:112252746..112254378,2	K562	blood:
33	chr5:112257473..112261765-chr5:112262739..112268514,7	K562	blood:
34	chr5:112252465..112254297-chr5:112272394..112274579,2	K562	blood:
35	chr5:112253344..112255730-chr5:112269581..112271953,2	MCF-7	breast:
36	chr5:112262263..112263764-chr5:112265083..112267354,2	K562	blood:
37	chr14:102543693..102544490-chr5:112257112..112258011,2	HCT-116	colon:
38	chr5:112253073..112255997-chr5:112284078..112285645,2	K562	blood:
39	chr5:112196028..112199860-chr5:112256680..112260462,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZRSR1-4	chr5:112268586-112268830	NONHSAT103252

No data

Variant related genes	Relation type
REEP5	TF binding region
REEP5	CpG island
ENSG00000166454	chromatin interactions
ENSG00000240457	chromatin interactions
ENSG00000212643	chromatin interactions
ENSG00000224032	chromatin interactions
ENSG00000238363	chromatin interactions
ENSG00000260213	chromatin interactions
ENSG00000272869	chromatin interactions
ENSG00000129625	chromatin interactions
ENSG00000153037	chromatin interactions
ENSG00000172795	chromatin interactions

Extended variants
information (count: 1355 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1355 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6882720	chr5:112254333-112254334	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143961044	chr5:112254334-112254335	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs370127538	chr5:112254335-112254336	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs184400541	chr5:112254367-112254368	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs153560	chr5:112254377-112254378	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs148212935	chr5:112254391-112254392	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs115906690	chr5:112254400-112254401	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs559918913	chr5:112254449-112254450	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs539214489	chr5:112254467-112254468	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs577019023	chr5:112254537-112254538	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs572166080	chr5:112254551-112254552	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs75330917	chr5:112254579-112254580	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs28410985	chr5:112254616-112254617	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs375241459	chr5:112254629-112254630	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs369213657	chr5:112254676-112254677	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs541778161	chr5:112254707-112254708	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs563151448	chr5:112254718-112254719	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs530791384	chr5:112254737-112254738	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs560461710	chr5:112254796-112254797	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs187302647	chr5:112254801-112254802	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs141192451	chr5:112254806-112254807	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs117901309	chr5:112254821-112254822	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs191692138	chr5:112254829-112254830	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs566159035	chr5:112254866-112254867	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs536371594	chr5:112254869-112254870	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs116221231	chr5:112254874-112254875	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs150780947	chr5:112254884-112254885	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs139655600	chr5:112254886-112254887	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs35296782	chr5:112254959-112254960	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs558975560	chr5:112254978-112254979	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs183956189	chr5:112254985-112254986	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs372924797	chr5:112255003-112255004	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs541201686	chr5:112255004-112255005	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553172267	chr5:112255008-112255009	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs189411034	chr5:112255029-112255030	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs1833560	chr5:112255072-112255073	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs145323304	chr5:112255098-112255099	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs370093857	chr5:112255105-112255106	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs575129820	chr5:112255106-112255107	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs192164957	chr5:112255118-112255119	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs147207416	chr5:112255119-112255120	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs528426212	chr5:112255138-112255139	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs185781068	chr5:112255172-112255173	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs139879346	chr5:112255173-112255174	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs530171417	chr5:112255179-112255180	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs536539225	chr5:112255198-112255199	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs153559	chr5:112255219-112255220	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs537032080	chr5:112255225-112255226	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs190258555	chr5:112255231-112255232	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs571907157	chr5:112255256-112255257	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Colorectal cancer	21297112	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Sezary syndrome	18413736	CNVD
Cancer	17440070	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:972 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:112211600-112256400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:112212200-112256400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr5:112215200-112255800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr5:112221800-112256600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:112222000-112256400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr5:112223000-112256400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr5:112223000-112256600	Weak transcription	Thymus	Thymus
8	chr5:112229600-112256600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr5:112242600-112256800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr5:112247800-112255800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr5:112248000-112255600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr5:112248200-112255600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr5:112248400-112256000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr5:112249400-112254400	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr5:112249400-112255600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr5:112250000-112254600	Strong transcription	H1 Cell Line	embryonic stem cell
17	chr5:112250200-112254400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr5:112250200-112254800	Genic enhancers	Brain Inferior Temporal Lobe	brain
19	chr5:112250800-112255400	Strong transcription	HMEC	breast
20	chr5:112251000-112256000	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr5:112251200-112255800	Strong transcription	A549	lung
22	chr5:112251200-112256000	Strong transcription	HUES64 Cell Line	embryonic stem cell
23	chr5:112251200-112256000	Genic enhancers	Primary T cells fromperipheralblood	blood
24	chr5:112251200-112256200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr5:112251400-112254400	Genic enhancers	Osteobl	bone
26	chr5:112251400-112254800	Genic enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr5:112251400-112255600	Genic enhancers	Dnd41	blood
28	chr5:112251400-112255800	Strong transcription	Fetal Stomach	stomach
29	chr5:112251400-112256000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr5:112251400-112256000	Genic enhancers	Monocytes-CD14+_RO01746	blood
31	chr5:112251600-112254800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
32	chr5:112251600-112255600	Strong transcription	NH-A	brain
33	chr5:112251600-112256000	Genic enhancers	Primary B cells from cord blood	blood
34	chr5:112251600-112256200	Strong transcription	HUES48 Cell Line	embryonic stem cell
35	chr5:112251600-112256200	Genic enhancers	Adipose Nuclei	Adipose
36	chr5:112251600-112256400	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr5:112251800-112254400	Genic enhancers	Colon Smooth Muscle	Colon
38	chr5:112251800-112254400	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
39	chr5:112251800-112254800	Genic enhancers	Primary T helper cells PMA-I stimulated	--
40	chr5:112251800-112255400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr5:112251800-112255400	Genic enhancers	Brain Anterior Caudate	brain
42	chr5:112251800-112255600	Genic enhancers	Left Ventricle	heart
43	chr5:112251800-112256000	Genic enhancers	Primary monocytes fromperipheralblood	blood
44	chr5:112252000-112254600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr5:112252000-112254600	Genic enhancers	Duodenum Mucosa	Duodenum
46	chr5:112252000-112255200	Genic enhancers	Fetal Brain Female	brain
47	chr5:112252000-112255400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr5:112252000-112255800	Strong transcription	HUES6 Cell Line	embryonic stem cell
49	chr5:112252200-112255200	Strong transcription	HUVEC	blood vessel
50	chr5:112252200-112255600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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