Variant report

Variant	nsv904220
Chromosome Location	chr15:52485024-52526507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:901)
CpG islands
(count:245)
Chromatin interactive
region (count:62)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:901 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:52500592-52500854	HepG2	liver:	n/a	n/a
2	ATF1	chr15:52519613-52520042	K562	blood:	n/a	n/a
3	ATF1	chr15:52521191-52521433	K562	blood:	n/a	n/a
4	ATF3	chr15:52521129-52521393	K562	blood:	n/a	chr15:52521286-52521294 chr15:52521286-52521306 chr15:52521283-52521296
5	BATF	chr15:52489172-52489416	GM12878	blood:	n/a	n/a
6	BATF	chr15:52524542-52524809	GM12878	blood:	n/a	n/a
7	BATF	chr15:52489171-52489400	GM12878	blood:	n/a	n/a
8	BATF	chr15:52524517-52524811	GM12878	blood:	n/a	n/a
9	BCLAF1	chr15:52524426-52524843	GM12878	blood:	n/a	chr15:52524688-52524697
10	BCLAF1	chr15:52524483-52524882	GM12878	blood:	n/a	chr15:52524688-52524697
11	BHLHE40	chr15:52521190-52521472	K562	blood:	n/a	n/a
12	BHLHE40	chr15:52509494-52509574	K562	blood:	n/a	n/a
13	BHLHE40	chr15:52514128-52514368	GM12878	blood:	n/a	n/a
14	BHLHE40	chr15:52521163-52521374	HepG2	liver:	n/a	n/a
15	BHLHE40	chr15:52500596-52500821	HepG2	liver:	n/a	n/a
16	BHLHE40	chr15:52513178-52513477	GM12878	blood:	n/a	n/a
17	BHLHE40	chr15:52524604-52524900	GM12878	blood:	n/a	n/a
18	BHLHE40	chr15:52519702-52519947	K562	blood:	n/a	n/a
19	BHLHE40	chr15:52519627-52519979	GM12878	blood:	n/a	n/a
20	CEBPB	chr15:52521128-52521388	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr15:52520982-52521540	A549	lung:	n/a	n/a
22	CEBPB	chr15:52521093-52521468	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr15:52489484-52489803	A549	lung:	n/a	chr15:52489775-52489786
24	CEBPB	chr15:52521123-52521515	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr15:52489704-52489816	HepG2	liver:	n/a	chr15:52489775-52489786
26	CEBPB	chr15:52520073-52520168	A549	lung:	n/a	n/a
27	CEBPB	chr15:52521094-52521542	MCF-7	breast:	n/a	n/a
28	CEBPB	chr15:52521115-52521578	MCF-7	breast:	n/a	n/a
29	CEBPB	chr15:52521128-52521449	K562	blood:	n/a	n/a
30	CEBPB	chr15:52521142-52521427	HepG2	liver:	n/a	n/a
31	CEBPB	chr15:52505734-52505930	IMR90	lung:	n/a	n/a
32	CEBPB	chr15:52521130-52521446	A549	lung:	n/a	n/a
33	CHD1	chr15:52513614-52514379	GM12878	blood:	n/a	n/a
34	CHD1	chr15:52525651-52525840	GM12878	blood:	n/a	n/a
35	CHD1	chr15:52519469-52520061	IMR90	lung:	n/a	n/a
36	CHD2	chr15:52524624-52524874	GM12878	blood:	n/a	n/a
37	CHD2	chr15:52519736-52519928	GM12878	blood:	n/a	n/a
38	CHD2	chr15:52525607-52525887	GM12878	blood:	n/a	n/a
39	CHD2	chr15:52513389-52513577	GM12878	blood:	n/a	n/a
40	CREB1	chr15:52521139-52521569	GM12878	blood:	n/a	n/a
41	CREB1	chr15:52521082-52521574	ECC-1	luminal epithelium:	n/a	n/a
42	CTCF	chr15:52500470-52500955	K562	blood:	n/a	chr15:52500726-52500739 chr15:52500651-52500660
43	CTCF	chr15:52509428-52509566	SK-N-SH_RA	brain:	n/a	chr15:52509509-52509530 chr15:52509507-52509525 chr15:52509510-52509523 chr15:52509510-52509523 chr15:52509508-52509524
44	CTCF	chr15:52500640-52500790	GM12874	blood:	n/a	chr15:52500726-52500739 chr15:52500651-52500660
45	CTCF	chr15:52509480-52509630	GM12867	blood:	n/a	chr15:52509509-52509530 chr15:52509507-52509525 chr15:52509510-52509523 chr15:52509510-52509523 chr15:52509508-52509524
46	CTCF	chr15:52509480-52509630	GM12866	blood:	n/a	chr15:52509509-52509530 chr15:52509507-52509525 chr15:52509510-52509523 chr15:52509510-52509523 chr15:52509508-52509524
47	CTCF	chr15:52500576-52500851	Fibrobl	skin:	n/a	chr15:52500726-52500739 chr15:52500651-52500660
48	CTCF	chr15:52516469-52516525	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr15:52519676-52519888	MCF-7	breast:	n/a	chr15:52519755-52519773 chr15:52519756-52519772 chr15:52519750-52519771
50	CTCF	chr15:52509440-52509590	HRPEpiC	eye:	n/a	chr15:52509509-52509530 chr15:52509507-52509525 chr15:52509510-52509523 chr15:52509510-52509523 chr15:52509508-52509524

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:52496988-52497038	HRE	kidney:	n/a
2	chr15:52496988-52497038	HRE	kidney:	n/a
3	chr15:52497132-52497182	Hela-S3	cervix:	n/a
4	chr15:52496988-52497038	BE2_C	brain:	n/a
5	chr15:52496988-52497038	PrEC	prostate:	n/a
6	chr15:52506363-52506413	Caco-2	colon:	n/a
7	chr15:52497132-52497182	PFSK-1	brain:	n/a
8	chr15:52497132-52497182	MCF10A-Er-Src	breast:	n/a
9	chr15:52496988-52497038	HRCEpiC	kidney:	n/a
10	chr15:52497340-52497390	GM19239	blood:	n/a
11	chr15:52497132-52497182	HCF	heart:	n/a
12	chr15:52497340-52497390	PrEC	prostate:	n/a
13	chr15:52497132-52497182	GM12891	blood:	n/a
14	chr15:52496988-52497038	AG09319	gingival:	n/a
15	chr15:52497340-52497390	RPTEC	kidney:	n/a
16	chr15:52506363-52506413	NH-A	brain:	n/a
17	chr15:52506363-52506413	GM12892	blood:	n/a
18	chr15:52497340-52497390	HL-60	blood:	n/a
19	chr15:52497340-52497390	MCF10A-Er-Src	breast:	n/a
20	chr15:52506363-52506413	HCF	heart:	n/a
21	chr15:52496988-52497038	RPTEC	kidney:	n/a
22	chr15:52496988-52497038	A549	lung:	n/a
23	chr15:52506363-52506413	A549	lung:	n/a
24	chr15:52496988-52497038	HIPEpiC	eye:	n/a
25	chr15:52496988-52497038	Hepatocyte	liver:	n/a
26	chr15:52496988-52497038	SAEC	small airway:	n/a
27	chr15:52506363-52506413	BE2_C	brain:	n/a
28	chr15:52497132-52497182	ovcar-3	ovarian:	n/a
29	chr15:52506363-52506413	HNPCEpiC	eye:	n/a
30	chr15:52497340-52497390	NHDF-neo	bronchial:	n/a
31	chr15:52506363-52506413	HRPEpiC	eye:	n/a
32	chr15:52496988-52497038	MCF-7	breast:	n/a
33	chr15:52497340-52497390	AG10803	skin:	n/a
34	chr15:52496988-52497038	ProgFib	skin:	n/a
35	chr15:52497340-52497390	SK-N-MC	brain:	n/a
36	chr15:52506363-52506413	MCF10A-Er-Src	breast:	n/a
37	chr15:52496988-52497038	HCPEpiC	choroid plexus:	n/a
38	chr15:52496988-52497038	Jurkat	blood:	n/a
39	chr15:52497340-52497390	T-47D	breast:	n/a
40	chr15:52496988-52497038	ovcar-3	ovarian:	n/a
41	chr15:52506363-52506413	AG09319	gingival:	n/a
42	chr15:52496988-52497038	GM12878	blood:	n/a
43	chr15:52496988-52497038	HL-60	blood:	n/a
44	chr15:52496988-52497038	Caco-2	colon:	n/a
45	chr15:52497340-52497390	Caco-2	colon:	n/a
46	chr15:52496988-52497038	AG09309	skin:	n/a
47	chr15:52506363-52506413	Jurkat	blood:	n/a
48	chr15:52497132-52497182	K562	blood:	n/a
49	chr15:52496988-52497038	AoSMC	blood vessel:	n/a
50	chr15:52497340-52497390	SKMC	muscle:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:52500850..52502666-chr15:52514026..52515788,2	MCF-7	breast:
2	chr15:52509089..52509941-chr15:53027516..53028325,2	MCF-7	breast:
3	chr15:52496666..52498415-chr15:52943182..52945600,2	MCF-7	breast:
4	chr15:52475563..52476065-chr15:52509089..52509975,2	MCF-7	breast:
5	chr15:52509233..52510844-chr15:52512535..52515103,2	K562	blood:
6	chr15:52490583..52493341-chr15:52495690..52497314,2	MCF-7	breast:
7	chr15:52510129..52510638-chr15:52519361..52520037,2	MCF-7	breast:
8	chr15:52487648..52490505-chr15:52490817..52493164,2	MCF-7	breast:
9	chr15:52473146..52475949-chr15:52491813..52494076,2	MCF-7	breast:
10	chr15:52455491..52456419-chr15:52500266..52500940,3	K562	blood:
11	chr15:52487648..52490505-chr15:52490817..52493164,2	MCF-7	breast:
12	chr15:52271043..52273593-chr15:52500641..52502378,2	MCF-7	breast:
13	chr15:52498552..52502035-chr15:52503246..52505472,3	MCF-7	breast:
14	chr15:52455479..52456330-chr15:52500106..52501199,5	MCF-7	breast:
15	chr15:52513190..52514784-chr15:52519152..52521403,2	MCF-7	breast:
16	chr15:52513190..52514784-chr15:52519152..52521403,2	MCF-7	breast:
17	chr15:52469037..52470714-chr15:52511840..52513591,2	MCF-7	breast:
18	chr15:52509083..52509697-chr15:53027309..53027962,2	MCF-7	breast:
19	chr15:52274239..52275037-chr15:52500239..52501186,3	MCF-7	breast:
20	chr15:52505434..52507299-chr15:52513137..52515697,2	MCF-7	breast:
21	chr15:52514548..52516962-chr15:52580174..52582493,2	MCF-7	breast:
22	chr15:52473218..52475845-chr15:52500048..52503534,3	MCF-7	breast:
23	chr15:52500676..52501391-chr15:52509036..52509975,2	K562	blood:
24	chr15:52499920..52501518-chr15:52503207..52505042,2	MCF-7	breast:
25	chr15:52477215..52477900-chr15:52500295..52500830,2	MCF-7	breast:
26	chr15:52480643..52483811-chr15:52484506..52486850,3	MCF-7	breast:
27	chr15:52521161..52523907-chr15:52528053..52529733,2	MCF-7	breast:
28	chr15:52477453..52480086-chr15:52495513..52498158,2	K562	blood:
29	chr15:52509010..52510015-chr15:52519316..52520083,4	MCF-7	breast:
30	chr15:52498552..52502035-chr15:52503246..52505472,3	MCF-7	breast:
31	chr15:52520877..52522858-chr15:52523295..52525074,3	MCF-7	breast:
32	chr15:52475319..52476508-chr15:52500260..52501551,7	MCF-7	breast:
33	chr15:52475538..52476921-chr15:52500216..52501095,4	MCF-7	breast:
34	chr15:52521390..52524844-chr15:52525282..52528513,3	MCF-7	breast:
35	chr15:52521390..52524844-chr15:52525282..52528513,3	MCF-7	breast:
36	chr15:52486663..52491950-chr15:52497424..52502756,7	MCF-7	breast:
37	chr15:52509233..52510844-chr15:52512535..52515103,2	K562	blood:
38	chr15:52490583..52493341-chr15:52495690..52497314,2	MCF-7	breast:
39	chr15:52519699..52521506-chr15:52579377..52581027,2	MCF-7	breast:
40	chr15:52486663..52491950-chr15:52497424..52502756,7	MCF-7	breast:
41	chr15:52466781..52469103-chr15:52500146..52502200,2	MCF-7	breast:
42	chr15:52510129..52510638-chr15:52519361..52520037,2	MCF-7	breast:
43	chr15:52505827..52511235-chr15:52516876..52519875,7	MCF-7	breast:
44	chr15:52485700..52488644-chr15:52493368..52494884,2	MCF-7	breast:
45	chr15:52216346..52217850-chr15:52500229..52502926,2	MCF-7	breast:
46	chr15:52499920..52501518-chr15:52503207..52505042,2	MCF-7	breast:
47	chr15:52471929..52473457-chr15:52519200..52522069,2	MCF-7	breast:
48	chr15:52508008..52509939-chr15:53026331..53028847,2	MCF-7	breast:
49	chr15:52500676..52501391-chr15:52509036..52509975,2	K562	blood:
50	chr15:52311257..52313666-chr15:52519365..52521577,2	MCF-7	breast:

No data

Variant related genes	Relation type
MYO5C	TF binding region
GNB5	TF binding region
MYO5C	CpG island
GNB5	CpG island
ENSG00000259438	chromatin interactions
ENSG00000138594	chromatin interactions
ENSG00000128833	chromatin interactions
ENSG00000069966	chromatin interactions
ENSG00000259577	chromatin interactions
ENSG00000047346	chromatin interactions
ENSG00000069956	chromatin interactions

Extended variants
information (count: 1613 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1613 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4219	chr15:52485024-52485025	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs577318245	chr15:52485038-52485039	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs74265743	chr15:52485062-52485063	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs398057687	chr15:52485064-52485065	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs56176906	chr15:52485066-52485067	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs148957716	chr15:52485089-52485090	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs539640849	chr15:52485102-52485103	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs201042522	chr15:52485110-52485111	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs569457117	chr15:52485153-52485154	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs143651607	chr15:52485162-52485163	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs374446673	chr15:52485229-52485230	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs12439660	chr15:52485235-52485236	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs182159612	chr15:52485262-52485263	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534182667	chr15:52485295-52485296	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs555761705	chr15:52485320-52485321	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs138266997	chr15:52485364-52485365	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs560883239	chr15:52485418-52485419	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs62016462	chr15:52485441-52485442	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs556053898	chr15:52485453-52485454	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs143753379	chr15:52485512-52485513	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs397854060	chr15:52485513-52485514	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs546017925	chr15:52485529-52485530	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs5812588	chr15:52485530-52485531	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs58273159	chr15:52485531-52485532	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs33976815	chr15:52485532-52485533	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs200591028	chr15:52485535-52485536	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs577417481	chr15:52485543-52485544	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs146041300	chr15:52485624-52485625	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs138769064	chr15:52485657-52485658	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs571854949	chr15:52485700-52485701	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs187210883	chr15:52485710-52485711	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs560955491	chr15:52485787-52485788	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs200344067	chr15:52485805-52485806	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs141231620	chr15:52485835-52485836	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs528291715	chr15:52485855-52485856	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs551260269	chr15:52485894-52485895	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs371323981	chr15:52485948-52485949	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs572316026	chr15:52486023-52486024	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs370994921	chr15:52486048-52486049	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs562903003	chr15:52486064-52486065	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs375258360	chr15:52486080-52486081	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs533558650	chr15:52486083-52486084	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs111952796	chr15:52486168-52486169	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs202130148	chr15:52486169-52486170	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs200612257	chr15:52486174-52486175	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs375234011	chr15:52486201-52486202	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs534320787	chr15:52486215-52486216	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs139087221	chr15:52486227-52486228	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs374653735	chr15:52486235-52486236	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs117839799	chr15:52486254-52486255	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:921 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:52473000-52489000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr15:52473200-52513600	Weak transcription	Rectal Smooth Muscle	rectum
3	chr15:52473400-52485600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr15:52473400-52496400	Weak transcription	Brain Anterior Caudate	brain
5	chr15:52473400-52496400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr15:52473400-52496600	Weak transcription	Spleen	Spleen
7	chr15:52473600-52512400	Weak transcription	Primary B cells from cord blood	blood
8	chr15:52474600-52488400	Weak transcription	Fetal Muscle Leg	muscle
9	chr15:52475800-52505600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr15:52477600-52497000	Weak transcription	Primary B cells from peripheral blood	blood
11	chr15:52477600-52497200	Weak transcription	Stomach Mucosa	stomach
12	chr15:52477800-52488000	Weak transcription	Gastric	stomach
13	chr15:52477800-52494800	Weak transcription	Fetal Intestine Large	intestine
14	chr15:52478000-52496200	Weak transcription	Liver	Liver
15	chr15:52478600-52488400	Weak transcription	Aorta	Aorta
16	chr15:52479600-52487400	Weak transcription	HepG2	liver
17	chr15:52479600-52495400	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr15:52479600-52496400	Weak transcription	Esophagus	oesophagus
19	chr15:52479800-52485600	Weak transcription	Ovary	ovary
20	chr15:52479800-52532800	Weak transcription	Brain Angular Gyrus	brain
21	chr15:52481400-52485600	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr15:52481600-52496600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr15:52482000-52485600	Weak transcription	Fetal Muscle Trunk	muscle
24	chr15:52482600-52496200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr15:52483400-52492400	Strong transcription	Rectal Mucosa Donor 29	rectum
26	chr15:52483600-52485600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr15:52483600-52485800	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr15:52483600-52485800	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr15:52483600-52488400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr15:52483600-52489200	Strong transcription	Rectal Mucosa Donor 31	rectum
31	chr15:52483600-52496400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr15:52483800-52485600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr15:52483800-52487200	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr15:52483800-52487200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr15:52483800-52487400	Weak transcription	Primary hematopoietic stem cells	blood
36	chr15:52483800-52487800	Weak transcription	Colonic Mucosa	Colon
37	chr15:52483800-52488400	Weak transcription	Fetal Stomach	stomach
38	chr15:52483800-52497000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr15:52484000-52485800	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr15:52484000-52492400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr15:52484200-52488200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr15:52484200-52488200	Weak transcription	Fetal Intestine Small	intestine
43	chr15:52484200-52488400	Weak transcription	Pancreas	Pancrea
44	chr15:52484200-52490600	Weak transcription	A549	lung
45	chr15:52484200-52496400	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr15:52484200-52497000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr15:52484200-52498600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr15:52484200-52503200	Weak transcription	Lung	lung
49	chr15:52484400-52487200	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr15:52484400-52503800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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