Variant report

Variant	nsv542320
Chromosome Location	chr15:31728004-31972706
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3288)
CpG islands
(count:1955)
Chromatin interactive
region (count:70)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3288 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:31931274-31931549	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:31780846-31781135	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:31780793-31781117	K562	blood:	n/a	n/a
4	ARID3A	chr15:31832931-31833126	HepG2	liver:	n/a	n/a
5	ATF1	chr15:31736055-31736373	K562	blood:	n/a	n/a
6	ATF1	chr15:31739062-31739258	K562	blood:	n/a	n/a
7	ATF1	chr15:31808762-31808962	K562	blood:	n/a	n/a
8	ATF2	chr15:31726982-31728063	GM12878	blood:	n/a	n/a
9	ATF2	chr15:31729885-31730244	GM12878	blood:	n/a	n/a
10	ATF2	chr15:31726850-31728137	GM12878	blood:	n/a	n/a
11	ATF2	chr15:31780042-31780621	GM12878	blood:	n/a	n/a
12	ATF2	chr15:31780255-31781128	GM12878	blood:	n/a	n/a
13	ATF2	chr15:31729778-31730296	GM12878	blood:	n/a	n/a
14	ATF2	chr15:31735877-31736427	GM12878	blood:	n/a	n/a
15	ATF2	chr15:31751038-31751815	GM12878	blood:	n/a	n/a
16	ATF2	chr15:31751192-31751725	GM12878	blood:	n/a	n/a
17	ATF2	chr15:31735790-31736388	GM12878	blood:	n/a	n/a
18	ATF3	chr15:31727560-31728064	GM12878	blood:	n/a	n/a
19	ATF3	chr15:31736109-31736314	K562	blood:	n/a	n/a
20	BACH1	chr15:31747847-31747986	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr15:31732960-31733542	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr15:31775531-31776385	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr15:31731640-31731907	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr15:31727556-31728056	GM12878	blood:	n/a	n/a
25	BATF	chr15:31783524-31783756	GM12878	blood:	n/a	n/a
26	BATF	chr15:31942586-31942812	GM12878	blood:	n/a	n/a
27	BATF	chr15:31735728-31736270	GM12878	blood:	n/a	chr15:31735937-31735947
28	BATF	chr15:31783531-31783735	GM12878	blood:	n/a	n/a
29	BATF	chr15:31727686-31728016	GM12878	blood:	n/a	n/a
30	BATF	chr15:31751257-31751640	GM12878	blood:	n/a	n/a
31	BATF	chr15:31780127-31781131	GM12878	blood:	n/a	chr15:31780490-31780500
32	BATF	chr15:31729899-31730241	GM12878	blood:	n/a	n/a
33	BATF	chr15:31780250-31780659	GM12878	blood:	n/a	chr15:31780490-31780500
34	BCL11A	chr15:31803930-31804280	GM12878	blood:	n/a	n/a
35	BCL11A	chr15:31942588-31942835	GM12878	blood:	n/a	n/a
36	BCL11A	chr15:31780237-31780696	GM12878	blood:	n/a	n/a
37	BCL11A	chr15:31751147-31751700	GM12878	blood:	n/a	n/a
38	BCL11A	chr15:31803961-31804201	GM12878	blood:	n/a	n/a
39	BCL11A	chr15:31780285-31780642	GM12878	blood:	n/a	n/a
40	BCL11A	chr15:31729850-31730246	GM12878	blood:	n/a	n/a
41	BCL3	chr15:31759025-31759318	GM12878	blood:	n/a	n/a
42	BCL3	chr15:31803945-31804250	GM12878	blood:	n/a	n/a
43	BCL3	chr15:31780314-31780731	GM12878	blood:	n/a	n/a
44	BCL3	chr15:31729832-31730220	GM12878	blood:	n/a	n/a
45	BCL3	chr15:31749134-31749475	GM12878	blood:	n/a	n/a
46	BCL3	chr15:31749116-31749537	GM12878	blood:	n/a	n/a
47	BCLAF1	chr15:31726852-31728065	GM12878	blood:	n/a	n/a
48	BCLAF1	chr15:31765120-31765606	GM12878	blood:	n/a	n/a
49	BCLAF1	chr15:31751116-31751769	GM12878	blood:	n/a	n/a
50	BHLHE40	chr15:31735818-31736245	GM12878	blood:	n/a	n/a

(count:1955 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31733445-31733495	GM19239	blood:	n/a
2	chr15:31775406-31775456	MCF10A-Er-Src	breast:	n/a
3	chr15:31745519-31745569	MCF-7	breast:	n/a
4	chr15:31733445-31733495	GM19239	blood:	n/a
5	chr15:31775406-31775456	MCF10A-Er-Src	breast:	n/a
6	chr15:31745519-31745569	MCF-7	breast:	n/a
7	chr15:31734262-31734312	A549	lung:	n/a
8	chr15:31745648-31745698	RPTEC	kidney:	n/a
9	chr15:31774773-31774823	GM12891	blood:	n/a
10	chr15:31733445-31733495	AG09319	gingival:	n/a
11	chr15:31734262-31734312	HRE	kidney:	n/a
12	chr15:31744207-31744257	GM12891	blood:	n/a
13	chr15:31745916-31745966	SK-N-SH	brain:	n/a
14	chr15:31846670-31846720	HCT-116	colon:	n/a
15	chr15:31742799-31742849	GM19239	blood:	n/a
16	chr15:31745894-31745944	NHDF-neo	bronchial:	n/a
17	chr15:31775049-31775099	NHDF-neo	bronchial:	n/a
18	chr15:31745519-31745569	Caco-2	colon:	n/a
19	chr15:31775049-31775099	HRPEpiC	eye:	n/a
20	chr15:31731005-31731055	NB4	blood:	n/a
21	chr15:31731005-31731055	ProgFib	skin:	n/a
22	chr15:31745519-31745569	AoSMC	blood vessel:	n/a
23	chr15:31745894-31745944	Caco-2	colon:	n/a
24	chr15:31732992-31733042	IMR90	lung:	fetal
25	chr15:31745648-31745698	MCF-7	breast:	n/a
26	chr15:31745729-31745779	AG04449	skin:	fetal
27	chr15:31776450-31776500	NB4	blood:	n/a
28	chr15:31745648-31745698	A549	lung:	n/a
29	chr15:31776450-31776500	MCF-7	breast:	n/a
30	chr15:31749573-31749623	GM12891	blood:	n/a
31	chr15:31742799-31742849	HIPEpiC	eye:	n/a
32	chr15:31775895-31775945	HepG2	liver:	n/a
33	chr15:31948632-31948682	HCM	heart:	n/a
34	chr15:31733101-31733151	AG10803	skin:	n/a
35	chr15:31898033-31898083	T-47D	breast:	n/a
36	chr15:31774976-31775026	A549	lung:	n/a
37	chr15:31733101-31733151	SK-N-MC	brain:	n/a
38	chr15:31737459-31737509	SK-N-SH_RA	brain:	n/a
39	chr15:31733485-31733535	HCF	heart:	n/a
40	chr15:31781955-31782005	HCM	heart:	n/a
41	chr15:31776450-31776500	Hela-S3	cervix:	n/a
42	chr15:31773057-31773107	Hela-S3	cervix:	n/a
43	chr15:31775406-31775456	HNPCEpiC	eye:	n/a
44	chr15:31733485-31733535	HRPEpiC	eye:	n/a
45	chr15:31731005-31731055	Hela-S3	cervix:	n/a
46	chr15:31948632-31948682	PANC-1	pancreas:	n/a
47	chr15:31776741-31776791	AG09309	skin:	n/a
48	chr15:31744207-31744257	ECC-1	luminal epithelium:	n/a
49	chr15:31777358-31777408	NHBE	bronchial:	n/a
50	chr15:31745916-31745966	Jurkat	blood:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:31727174..31728141-chr20:58146623..58147201,2	MCF-7	breast:
2	chr15:31729614..31735490-chr15:31778794..31782835,6	MCF-7	breast:
3	chr15:31748477..31753108-chr15:31776889..31783172,7	MCF-7	breast:
4	chr15:31595209..31595834-chr15:31726996..31728128,4	MCF-7	breast:
5	chr15:31492924..31493816-chr15:31781800..31782800,3	K562	blood:
6	chr15:31753115..31755985-chr15:31766097..31768042,2	MCF-7	breast:
7	chr15:31753960..31755078-chr15:31780591..31781425,3	MCF-7	breast:
8	chr15:31727509..31730318-chr15:31731392..31734401,4	MCF-7	breast:
9	chr15:31492529..31493483-chr15:31780441..31781476,6	MCF-7	breast:
10	chr15:31507689..31508257-chr15:31779754..31780346,2	K562	blood:
11	chr15:31747904..31750478-chr15:31754531..31757245,2	MCF-7	breast:
12	chr15:31730274..31733204-chr15:32160841..32163038,2	MCF-7	breast:
13	chr1:149222127..149223797-chr15:31897038..31899511,2	MCF-7	breast:
14	chr15:31731428..31732434-chr15:31780398..31781184,5	K562	blood:
15	chr15:31860388..31862871-chr15:31898549..31900652,2	MCF-7	breast:
16	chr15:31730666..31732248-chr15:31779741..31781482,12	MCF-7	breast:
17	chr15:31731861..31735385-chr15:31748681..31751856,6	MCF-7	breast:
18	chr15:31507577..31508378-chr15:31727245..31728255,4	MCF-7	breast:
19	chr15:31780894..31782465-chr15:31785232..31787543,2	MCF-7	breast:
20	chr15:31731861..31735385-chr15:31748681..31751856,6	MCF-7	breast:
21	chr15:31658522..31659115-chr15:31727119..31728025,2	MCF-7	breast:
22	chr15:31753081..31754904-chr15:31769113..31772729,3	MCF-7	breast:
23	chr15:31727262..31728165-chr15:31780632..31781327,2	MCF-7	breast:
24	chr15:31732939..31734910-chr15:31736139..31739107,2	MCF-7	breast:
25	chr15:31616708..31620581-chr15:31726270..31733622,8	MCF-7	breast:
26	chr15:31492707..31493313-chr15:31780465..31781069,2	MCF-7	breast:
27	chr15:31819613..31821709-chr15:31823051..31825388,2	K562	blood:
28	chr15:31727509..31730318-chr15:31731392..31734401,4	MCF-7	breast:
29	chr15:31863635..31864490-chr15:32159813..32160454,2	MCF-7	breast:
30	chr15:31492737..31493697-chr15:31726904..31728527,12	MCF-7	breast:
31	chr15:31507301..31508500-chr15:31780431..31781449,6	K562	blood:
32	chr15:31507326..31508291-chr15:31727308..31728255,4	MCF-7	breast:
33	chr15:31860388..31862871-chr15:31898549..31900652,2	MCF-7	breast:
34	chr15:31507741..31508382-chr15:31730961..31731952,2	K562	blood:
35	chr15:31617973..31620260-chr15:31730355..31732158,2	MCF-7	breast:
36	chr15:31768996..31771688-chr15:31773371..31775681,2	MCF-7	breast:
37	chr15:31753081..31754904-chr15:31769113..31772729,3	MCF-7	breast:
38	chr15:31875085..31876588-chr15:31881035..31883646,2	K562	blood:
39	chr15:31780894..31782465-chr15:31785232..31787543,2	MCF-7	breast:
40	chr15:31731428..31732434-chr15:31780398..31781184,5	K562	blood:
41	chr15:31489768..31490355-chr15:31780489..31781405,2	K562	blood:
42	chr15:31507500..31508054-chr15:31782035..31782545,2	K562	blood:
43	chr15:31748477..31753108-chr15:31776889..31783172,7	MCF-7	breast:
44	chr15:31753115..31755985-chr15:31766097..31768042,2	MCF-7	breast:
45	chr15:31637997..31638658-chr15:31727655..31728625,2	MCF-7	breast:
46	chr15:31729614..31735490-chr15:31778794..31782835,6	MCF-7	breast:
47	chr15:31768996..31771688-chr15:31773371..31775681,2	MCF-7	breast:
48	chr15:31875085..31876588-chr15:31881035..31883646,2	K562	blood:
49	chr15:31863857..31864715-chr15:32266784..32267619,2	MCF-7	breast:
50	chr15:31728928..31731704-chr15:31776995..31778781,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLF13-2	chr15:31817303-31817589	NONHSAT041464
2	lnc-KLF13-2	chr15:31814262-31814687	NONHSAT041464
3	lnc-KLF13-2	chr15:31815582-31816079	NONHSAT041465
4	lnc-KLF13-2	chr15:31817303-31817589	NONHSAT041465
5	lnc-KLF13-2	chr15:31815904-31816079	NONHSAT041464
6	lnc-OTUD7A-1	chr15:31767607-31770705	NONHSAT041463

No data

Variant related genes	Relation type
ENSG00000259696	TF binding region
OTUD7A	TF binding region
ENSG00000259696	CpG island
OTUD7A	CpG island
ENSG00000136709	chromatin interactions
ENSG00000169918	chromatin interactions
ENSG00000169926	chromatin interactions
ENSG00000259448	chromatin interactions

Extended variants
information (count: 9540 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:9540 , 50 per page) page: 1 2 3 4 5 6 7 ... 191

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187174451	chr15:31728006-31728007	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs141680752	chr15:31728011-31728012	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs75909491	chr15:31728020-31728021	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs577822525	chr15:31728068-31728069	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs192688137	chr15:31728090-31728091	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs184486740	chr15:31728103-31728104	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs543237344	chr15:31728113-31728114	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs529004799	chr15:31728134-31728135	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs149390905	chr15:31728159-31728160	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs12909199	chr15:31728163-31728164	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs534854568	chr15:31728179-31728180	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs375741081	chr15:31728206-31728207	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs562304977	chr15:31728284-31728285	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs12905351	chr15:31728344-31728345	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs144796713	chr15:31728345-31728346	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs551146231	chr15:31728351-31728352	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs113528612	chr15:31728361-31728362	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs150584261	chr15:31728362-31728363	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs12903529	chr15:31728372-31728373	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs377503014	chr15:31728378-31728379	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs148103827	chr15:31728391-31728392	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs545456983	chr15:31728392-31728393	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs546696035	chr15:31728400-31728401	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs566836708	chr15:31728430-31728431	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs557914888	chr15:31728452-31728453	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs535609140	chr15:31728477-31728478	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs4779875	chr15:31728508-31728509	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs568757648	chr15:31728525-31728526	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs537654329	chr15:31728556-31728557	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs141883136	chr15:31728591-31728592	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs577876462	chr15:31728599-31728600	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs367810408	chr15:31728652-31728653	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs12592287	chr15:31728696-31728697	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs35642570	chr15:31728790-31728791	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs534066868	chr15:31728812-31728813	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs553518761	chr15:31728829-31728830	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs572659146	chr15:31728830-31728831	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs543379677	chr15:31728834-31728835	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs111533108	chr15:31728835-31728836	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs372876739	chr15:31728839-31728840	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs59698969	chr15:31728841-31728842	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs561562892	chr15:31728868-31728869	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs374839606	chr15:31728923-31728924	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs564671401	chr15:31729015-31729016	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs533481570	chr15:31729039-31729040	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs140024301	chr15:31729079-31729080	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs560325567	chr15:31729129-31729130	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs529246093	chr15:31729134-31729135	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs548919897	chr15:31729138-31729139	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs75659929	chr15:31729162-31729163	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	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
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Epilepsy	20502679	CNVD
small cell lung cancer	20016488	CNVD
Autism	19521722	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Pancreatic cancer	17952125	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD
Schizophrenia	23813976	CNVD
Autism	21865298	CNVD

Chromatin state (count:2794 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31712800-31732800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:31725200-31728200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr15:31725400-31729000	Enhancers	Lung	lung
4	chr15:31725600-31728800	Enhancers	Esophagus	oesophagus
5	chr15:31726000-31731200	Enhancers	Spleen	Spleen
6	chr15:31726200-31728600	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr15:31726400-31728200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
8	chr15:31726400-31728200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
9	chr15:31726400-31728400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
10	chr15:31726400-31728600	Flanking Active TSS	GM12878-XiMat	blood
11	chr15:31726400-31728800	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr15:31726400-31728800	Enhancers	Small Intestine	intestine
13	chr15:31726600-31728200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr15:31726600-31728200	Flanking Active TSS	Primary T cells from cord blood	blood
15	chr15:31726600-31728600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr15:31726600-31728800	Flanking Active TSS	Dnd41	blood
17	chr15:31726600-31729000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
18	chr15:31726800-31728200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr15:31726800-31728200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
20	chr15:31726800-31728200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
21	chr15:31726800-31728200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
22	chr15:31726800-31728200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
23	chr15:31726800-31728200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr15:31726800-31728200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
25	chr15:31726800-31728200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
26	chr15:31726800-31728200	Flanking Active TSS	NH-A	brain
27	chr15:31726800-31728600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr15:31727000-31728200	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr15:31727000-31728200	Flanking Active TSS	Primary B cells from cord blood	blood
30	chr15:31727000-31728200	Enhancers	Muscle Satellite Cultured Cells	--
31	chr15:31727000-31728200	Flanking Active TSS	Adipose Nuclei	Adipose
32	chr15:31727000-31728200	Enhancers	Left Ventricle	heart
33	chr15:31727000-31728200	Enhancers	HMEC	breast
34	chr15:31727000-31728200	Flanking Active TSS	NHDF-Ad	bronchial
35	chr15:31727000-31728400	Enhancers	Fetal Muscle Trunk	muscle
36	chr15:31727200-31728200	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr15:31727200-31728200	Enhancers	Brain Substantia Nigra	brain
38	chr15:31727200-31728200	Enhancers	Fetal Heart	heart
39	chr15:31727400-31728200	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr15:31727400-31728200	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr15:31727400-31728200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr15:31727400-31728200	Flanking Active TSS	Liver	Liver
43	chr15:31727400-31728200	Flanking Active TSS	Duodenum Mucosa	Duodenum
44	chr15:31727400-31728200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr15:31727400-31728200	Flanking Active TSS	Stomach Smooth Muscle	stomach
46	chr15:31727400-31728200	Enhancers	HSMM	muscle
47	chr15:31727600-31728200	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr15:31727600-31728200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr15:31727600-31728200	Enhancers	Fetal Stomach	stomach
50	chr15:31727600-31728200	Flanking Active TSS	A549	lung

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