Variant report

Variant	esv3374779
Chromosome Location	chr15:40211885-40214433
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:40213584-40213598	K562	blood:	n/a	n/a
2	ATF2	chr15:40212646-40213505	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr15:40213055-40213300	HepG2	liver:	n/a	chr15:40213153-40213162 chr15:40213175-40213195
4	ATF3	chr15:40213019-40213368	H1-hESC	embryonic stem cell:	n/a	chr15:40213153-40213162 chr15:40213175-40213195
5	ATF3	chr15:40212987-40213349	K562	blood:	n/a	chr15:40213153-40213162 chr15:40213175-40213195
6	BACH1	chr15:40212357-40213516	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr15:40212964-40213444	K562	blood:	n/a	chr15:40213173-40213186 chr15:40213205-40213221 chr15:40213143-40213159 chr15:40213213-40213229
8	BHLHE40	chr15:40212974-40213463	GM12878	blood:	n/a	chr15:40213173-40213186 chr15:40213205-40213221 chr15:40213143-40213159 chr15:40213213-40213229
9	BHLHE40	chr15:40213016-40213416	HepG2	liver:	n/a	chr15:40213173-40213186 chr15:40213205-40213221 chr15:40213143-40213159 chr15:40213213-40213229
10	BRCA1	chr15:40212171-40212172	GM12878	blood:	n/a	n/a
11	BRCA1	chr15:40213002-40213005	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr15:40213156-40213541	K562	blood:	n/a	n/a
13	CBX3	chr15:40212487-40212892	K562	blood:	n/a	n/a
14	CBX3	chr15:40212976-40213501	K562	blood:	n/a	n/a
15	CCNT2	chr15:40212951-40213473	K562	blood:	n/a	chr15:40213193-40213202
16	CEBPB	chr15:40213784-40214084	IMR90	lung:	n/a	n/a
17	CEBPB	chr15:40213771-40214084	K562	blood:	n/a	n/a
18	CHD1	chr15:40212898-40213494	GM12878	blood:	n/a	chr15:40213198-40213208 chr15:40212983-40212990
19	CHD1	chr15:40210279-40213585	H1-hESC	embryonic stem cell:	n/a	chr15:40213198-40213208 chr15:40212983-40212990
20	CHD2	chr15:40212902-40213124	H1-hESC	embryonic stem cell:	n/a	chr15:40212983-40212990
21	CHD2	chr15:40213252-40213412	K562	blood:	n/a	n/a
22	CHD2	chr15:40212980-40213446	Hela-S3	cervix:	n/a	chr15:40213198-40213208 chr15:40212983-40212990
23	CHD2	chr15:40212747-40212761	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr15:40212494-40212654	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr15:40213069-40213400	GM12878	blood:	n/a	chr15:40213198-40213208
26	CREB1	chr15:40212888-40213352	A549	lung:	n/a	chr15:40213173-40213186
27	CTBP2	chr15:40211745-40213391	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr15:40212480-40212630	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr15:40212640-40212790	HFF	foreskin:	n/a	n/a
30	CTCF	chr15:40212480-40212630	HCFaa	heart:	n/a	n/a
31	CTCF	chr15:40212620-40212770	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr15:40213033-40213283	GM19239	blood:	n/a	chr15:40213145-40213158
33	CTCF	chr15:40212900-40213050	AG09319	gingival:	n/a	n/a
34	CTCF	chr15:40213200-40213350	BJ	skin:	n/a	n/a
35	CTCF	chr15:40213072-40213272	A549	lung:	n/a	chr15:40213145-40213158
36	CTCF	chr15:40213044-40213152	Medullo	brain:	n/a	n/a
37	CTCF	chr15:40212512-40212666	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr15:40212520-40212670	GM12872	blood:	n/a	n/a
39	CTCF	chr15:40212500-40212650	WI-38	lung:	n/a	n/a
40	CTCF	chr15:40212940-40213090	Caco-2	colon:	n/a	n/a
41	CTCF	chr15:40212760-40212910	HRE	kidney:	n/a	n/a
42	CTCF	chr15:40212980-40213130	Caco-2	colon:	n/a	n/a
43	CTCF	chr15:40213067-40213206	LNCaP	prostate:	n/a	chr15:40213145-40213158
44	CTCF	chr15:40212500-40212650	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr15:40212900-40213050	GM12867	blood:	n/a	n/a
46	CTCF	chr15:40212560-40212710	HVMF	connective:	n/a	n/a
47	CTCF	chr15:40212500-40212650	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr15:40213078-40213166	GM13977	blood:	n/a	chr15:40213145-40213158
49	CTCF	chr15:40212404-40213226	IMR90	lung:	n/a	chr15:40212458-40212476 chr15:40213145-40213158 chr15:40212461-40212474 chr15:40212460-40212481
50	CTCF	chr15:40212560-40212710	HRPEpiC	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:40212188-40212238	GM12878	blood:	n/a
2	chr15:40212188-40212238	GM12878	blood:	n/a
3	chr15:40213339-40213389	NT2-D1	testis:	n/a
4	chr15:40213326-40213376	NH-A	brain:	n/a
5	chr15:40212502-40212552	NH-A	brain:	n/a
6	chr15:40212188-40212238	HEK293	kidney:	embryo
7	chr15:40213314-40213364	AoSMC	blood vessel:	n/a
8	chr15:40212188-40212238	PANC-1	pancreas:	n/a
9	chr15:40213280-40213330	SKMC	muscle:	n/a
10	chr15:40213280-40213330	SAEC	small airway:	n/a
11	chr15:40212176-40212226	ProgFib	skin:	n/a
12	chr15:40212502-40212552	BE2_C	brain:	n/a
13	chr15:40212502-40212552	HNPCEpiC	eye:	n/a
14	chr15:40213280-40213330	HNPCEpiC	eye:	n/a
15	chr15:40213314-40213364	SK-N-SH_RA	brain:	n/a
16	chr15:40212781-40212831	HCT-116	colon:	n/a
17	chr15:40212106-40212156	HEEpiC	esophagus:	n/a
18	chr15:40213409-40213459	AG09309	skin:	n/a
19	chr15:40212106-40212156	Jurkat	blood:	n/a
20	chr15:40214068-40214118	NHBE	bronchial:	n/a
21	chr15:40213314-40213364	AG10803	skin:	n/a
22	chr15:40213409-40213459	ECC-1	luminal epithelium:	n/a
23	chr15:40212502-40212552	HRPEpiC	eye:	n/a
24	chr15:40213409-40213459	HepG2	liver:	n/a
25	chr15:40212502-40212552	GM19239	blood:	n/a
26	chr15:40212781-40212831	NH-A	brain:	n/a
27	chr15:40213326-40213376	ProgFib	skin:	n/a
28	chr15:40212176-40212226	GM12878	blood:	n/a
29	chr15:40212502-40212552	ECC-1	luminal epithelium:	n/a
30	chr15:40212176-40212226	Hepatocyte	liver:	n/a
31	chr15:40213280-40213330	ovcar-3	ovarian:	n/a
32	chr15:40214068-40214118	NHDF-neo	bronchial:	n/a
33	chr15:40212176-40212226	HCPEpiC	choroid plexus:	n/a
34	chr15:40213409-40213459	HEK293	kidney:	embryo
35	chr15:40213280-40213330	NB4	blood:	n/a
36	chr15:40213280-40213330	SK-N-SH	brain:	n/a
37	chr15:40213339-40213389	AG09319	gingival:	n/a
38	chr15:40213270-40213320	AG09309	skin:	n/a
39	chr15:40213314-40213364	Hela-S3	cervix:	n/a
40	chr15:40213270-40213320	CMK	blood:	n/a
41	chr15:40212781-40212831	HMEC	breast:	n/a
42	chr15:40212176-40212226	HEK293	kidney:	embryo
43	chr15:40213409-40213459	K562	blood:	n/a
44	chr15:40214068-40214118	BJ	skin:	n/a
45	chr15:40213270-40213320	GM12891	blood:	n/a
46	chr15:40212176-40212226	Jurkat	blood:	n/a
47	chr15:40212106-40212156	NHDF-neo	bronchial:	n/a
48	chr15:40212106-40212156	NT2-D1	testis:	n/a
49	chr15:40213314-40213364	GM06990	blood:	n/a
50	chr15:40213280-40213330	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:40211366..40214080-chr15:40223428..40228644,6	MCF-7	breast:
2	chr1:204042666..204043286-chr15:40213090..40213711,2	Hela-S3	cervix:
3	chr15:40213124..40213699-chr17:67323085..67323765,2	Hela-S3	cervix:
4	chr15:40211846..40214390-chr15:40224576..40226655,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2AK4-1	chr15:40213228-40213887	XLOC_011218
2	lnc-EIF2AK4-1	chr15:40213243-40213859	ENSG00000246863.2
3	lnc-EIF2AK4-1	chr15:40213271-40218081	ENSG00000246863.2
4	lnc-EIF2AK4-1	chr15:40213228-40213748	XLOC_011218
5	lnc-EIF2AK4-1	chr15:40213243-40213859	ENSG00000246863
6	lnc-EIF2AK4-1	chr15:40213228-40213743	XLOC_011218

Variant related genes	Relation type
GPR176	TF binding region
ENSG00000246863	TF binding region
GPR176	CpG island
ENSG00000246863	CpG island
ENSG00000128829	chromatin interactions
ENSG00000154265	chromatin interactions
ENSG00000143842	chromatin interactions
ERBB4	miRNA target sites
MYBL1	miRNA target sites

Extended variants
information (count: 111 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:111 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542825541	chr15:40211901-40211902	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs56107310	chr15:40211934-40211935	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs528818094	chr15:40211963-40211964	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs375099528	chr15:40211967-40211968	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs12912357	chr15:40211985-40211986	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs551779445	chr15:40211989-40211990	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs12912359	chr15:40211990-40211991	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs370363084	chr15:40212008-40212009	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs570476659	chr15:40212017-40212018	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs532793751	chr15:40212021-40212022	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs77245879	chr15:40212031-40212032	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs80137374	chr15:40212050-40212051	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs535515092	chr15:40212062-40212063	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs555628598	chr15:40212071-40212072	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs377215097	chr15:40212075-40212076	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs143700851	chr15:40212084-40212085	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs148093550	chr15:40212098-40212099	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs34575072	chr15:40212104-40212105	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs368646413	chr15:40212137-40212138	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs182145795	chr15:40212160-40212161	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs141122559	chr15:40212174-40212175	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs556899221	chr15:40212177-40212178	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs573815936	chr15:40212199-40212200	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs200109400	chr15:40212202-40212203	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs372442129	chr15:40212204-40212205	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs559563401	chr15:40212282-40212283	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs528676199	chr15:40212292-40212293	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs545538455	chr15:40212309-40212310	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs114232197	chr15:40212376-40212377	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs146865015	chr15:40212472-40212473	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs549824640	chr15:40212491-40212492	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs533235775	chr15:40212536-40212537	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs140235182	chr15:40212559-40212560	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs529033003	chr15:40212567-40212568	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs549088969	chr15:40212579-40212580	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs565912123	chr15:40212602-40212603	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs534519246	chr15:40212661-40212662	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs551511427	chr15:40212698-40212699	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs187253692	chr15:40212740-40212741	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs66690776	chr15:40212770-40212771	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs556974397	chr15:40212801-40212802	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs573691803	chr15:40212803-40212804	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs536397253	chr15:40212805-40212806	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs369444353	chr15:40212826-40212827	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs553055631	chr15:40212830-40212831	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs472530	chr15:40212834-40212835	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs545288680	chr15:40212898-40212899	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs146458017	chr15:40212934-40212935	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs575877317	chr15:40212960-40212961	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs544904975	chr15:40213074-40213075	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
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
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21129771	CNVD
Breast cancer	21045282	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Ovarian cancer	21720365	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD

Chromatin state (count:444 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40209000-40212400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr15:40209200-40213400	Active TSS	HUES48 Cell Line	embryonic stem cell
3	chr15:40209200-40213800	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr15:40209800-40213800	Active TSS	H1 Cell Line	embryonic stem cell
5	chr15:40210000-40212400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr15:40210000-40213600	Active TSS	H9 Cell Line	embryonic stem cell
7	chr15:40210200-40212600	Active TSS	Breast Myoepithelial Primary Cells	Breast
8	chr15:40210200-40212800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
9	chr15:40210200-40213600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr15:40210200-40213600	Active TSS	NHLF	lung
11	chr15:40210400-40212800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
12	chr15:40210400-40213400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr15:40210400-40213400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
14	chr15:40210400-40213600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr15:40210400-40213600	Active TSS	Aorta	Aorta
16	chr15:40210400-40213800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
17	chr15:40210600-40212600	Active TSS	HMEC	breast
18	chr15:40210600-40212800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr15:40210600-40213000	Active TSS	NH-A	brain
20	chr15:40210600-40213800	Active TSS	HSMM	muscle
21	chr15:40210800-40212600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
22	chr15:40210800-40212800	Active TSS	Muscle Satellite Cultured Cells	--
23	chr15:40210800-40213400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr15:40210800-40213400	Active TSS	HSMMtube	muscle
25	chr15:40210800-40213600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr15:40210800-40213600	Active TSS	NHDF-Ad	bronchial
27	chr15:40210800-40213800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr15:40211000-40212400	Active TSS	Brain Inferior Temporal Lobe	brain
29	chr15:40211000-40212600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
30	chr15:40211000-40212600	Bivalent/Poised TSS	A549	lung
31	chr15:40211000-40212800	Bivalent/Poised TSS	Fetal Brain Female	brain
32	chr15:40211000-40213000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
33	chr15:40211000-40213400	Active TSS	Osteobl	bone
34	chr15:40211000-40213600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr15:40211000-40213600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr15:40211000-40213600	Active TSS	Brain Anterior Caudate	brain
37	chr15:40211200-40212000	Bivalent Enhancer	Fetal Heart	heart
38	chr15:40211200-40212000	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
39	chr15:40211200-40212000	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
40	chr15:40211200-40212400	Active TSS	Brain Cingulate Gyrus	brain
41	chr15:40211200-40212400	Active TSS	Ovary	ovary
42	chr15:40211200-40212400	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
43	chr15:40211200-40213000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr15:40211200-40213600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr15:40211200-40213600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr15:40211200-40213800	Active TSS	Brain Angular Gyrus	brain
47	chr15:40211200-40213800	Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr15:40211400-40212000	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr15:40211400-40212200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
50	chr15:40211400-40212200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain

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