Variant report

Variant	esv3421724
Chromosome Location	chr14:64319224-64321772
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:555)
CpG islands
(count:490)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:555 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr14:64319119-64319461	GM12878	blood:	n/a	n/a
2	BHLHE40	chr14:64320253-64320376	K562	blood:	n/a	n/a
3	BHLHE40	chr14:64320654-64320953	GM12878	blood:	n/a	n/a
4	BHLHE40	chr14:64320179-64320341	HepG2	liver:	n/a	chr14:64320182-64320198
5	BHLHE40	chr14:64320113-64320436	GM12878	blood:	n/a	chr14:64320182-64320198
6	BRCA1	chr14:64320590-64321133	Hela-S3	cervix:	n/a	chr14:64320623-64320630
7	BRCA1	chr14:64320968-64321079	GM12878	blood:	n/a	n/a
8	CCNT2	chr14:64320126-64320398	K562	blood:	n/a	n/a
9	CEBPB	chr14:64319571-64319813	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr14:64320750-64320938	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr14:64320622-64320926	Hela-S3	cervix:	n/a	n/a
12	CHD1	chr14:64319631-64319792	H1-hESC	embryonic stem cell:	n/a	chr14:64319776-64319783 chr14:64319670-64319680
13	CHD1	chr14:64320555-64321411	GM12878	blood:	n/a	n/a
14	CHD1	chr14:64320146-64320354	GM12878	blood:	n/a	n/a
15	CHD2	chr14:64320959-64320976	GM12878	blood:	n/a	n/a
16	CHD2	chr14:64320641-64320850	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr14:64320775-64320807	HepG2	liver:	n/a	n/a
18	CHD2	chr14:64320055-64320347	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr14:64319487-64319824	Hela-S3	cervix:	n/a	chr14:64319776-64319783 chr14:64319670-64319680
20	CREB1	chr14:64319984-64320511	A549	lung:	n/a	n/a
21	CREB1	chr14:64319426-64319954	A549	lung:	n/a	n/a
22	CREB1	chr14:64320172-64320390	A549	lung:	n/a	n/a
23	CTBP2	chr14:64319088-64319839	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr14:64319560-64319710	NHLF	lung:	n/a	n/a
25	CTCF	chr14:64319300-64319450	HMF	breast:	n/a	n/a
26	CTCF	chr14:64319460-64319610	GM12873	blood:	n/a	n/a
27	CTCF	chr14:64319552-64319692	MCF-7	breast:	n/a	n/a
28	CTCF	chr14:64320023-64320215	Spleen_OC	spleen:	n/a	chr14:64320111-64320124
29	CTCF	chr14:64320000-64320150	MCF-7	breast:	n/a	chr14:64320111-64320124
30	CTCF	chr14:64320000-64320150	GM12871	blood:	n/a	chr14:64320111-64320124
31	CTCF	chr14:64320080-64320230	NHDF-neo	bronchial:	n/a	chr14:64320111-64320124
32	CTCF	chr14:64320020-64320170	HepG2	liver:	n/a	chr14:64320111-64320124
33	CTCF	chr14:64319980-64320130	HRE	kidney:	n/a	chr14:64320111-64320124
34	CTCF	chr14:64320258-64320260	GM19240	blood:	n/a	n/a
35	CTCF	chr14:64319580-64319631	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr14:64319540-64319690	GM12866	blood:	n/a	n/a
37	CTCF	chr14:64319260-64319410	HCFaa	heart:	n/a	n/a
38	CTCF	chr14:64320645-64320850	GM12878	blood:	n/a	n/a
39	CTCF	chr14:64319529-64319727	GM13976	blood:	n/a	n/a
40	CTCF	chr14:64319540-64319690	AG04449	skin:	n/a	n/a
41	CTCF	chr14:64319500-64319650	GM12872	blood:	n/a	n/a
42	CTCF	chr14:64319480-64319630	GM12864	blood:	n/a	n/a
43	CTCF	chr14:64319481-64319762	HepG2	liver:	n/a	n/a
44	CTCF	chr14:64319380-64319878	K562	blood:	n/a	n/a
45	CTCF	chr14:64319500-64319650	GM12870	blood:	n/a	n/a
46	CTCF	chr14:64319580-64319730	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr14:64320040-64320160	IMR90	lung:	n/a	chr14:64320111-64320124
48	CTCF	chr14:64319480-64319630	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr14:64319560-64319710	GM12878	blood:	n/a	n/a
50	CTCF	chr14:64320013-64320212	MCF-7	breast:	n/a	chr14:64320111-64320124

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:64320118-64320168	HRE	kidney:	n/a
2	chr14:64320118-64320168	HCM	heart:	n/a
3	chr14:64320118-64320168	HRE	kidney:	n/a
4	chr14:64320118-64320168	HCM	heart:	n/a
5	chr14:64319543-64319593	MCF10A-Er-Src	breast:	n/a
6	chr14:64319245-64319295	T-47D	breast:	n/a
7	chr14:64320521-64320571	ECC-1	luminal epithelium:	n/a
8	chr14:64320118-64320168	MCF-7	breast:	n/a
9	chr14:64319275-64319325	SAEC	small airway:	n/a
10	chr14:64319306-64319356	ProgFib	skin:	n/a
11	chr14:64319812-64319862	HEK293	kidney:	embryo
12	chr14:64320521-64320571	NHDF-neo	bronchial:	n/a
13	chr14:64320118-64320168	HUVEC	blood vessel:	n/a
14	chr14:64319812-64319862	RPTEC	kidney:	n/a
15	chr14:64320521-64320571	AG04450	lung:	fetal
16	chr14:64319543-64319593	HCPEpiC	choroid plexus:	n/a
17	chr14:64319275-64319325	RPTEC	kidney:	n/a
18	chr14:64319812-64319862	Caco-2	colon:	n/a
19	chr14:64320521-64320571	GM06990	blood:	n/a
20	chr14:64319812-64319862	AG04449	skin:	fetal
21	chr14:64319275-64319325	AG09319	gingival:	n/a
22	chr14:64320118-64320168	Caco-2	colon:	n/a
23	chr14:64320049-64320099	HIPEpiC	eye:	n/a
24	chr14:64319245-64319295	HEK293	kidney:	embryo
25	chr14:64319275-64319325	Caco-2	colon:	n/a
26	chr14:64319812-64319862	SK-N-MC	brain:	n/a
27	chr14:64320049-64320099	HEEpiC	esophagus:	n/a
28	chr14:64319306-64319356	HL-60	blood:	n/a
29	chr14:64319245-64319295	HepG2	liver:	n/a
30	chr14:64320118-64320168	NH-A	brain:	n/a
31	chr14:64319543-64319593	ECC-1	luminal epithelium:	n/a
32	chr14:64320521-64320571	GM19239	blood:	n/a
33	chr14:64319306-64319356	HCM	heart:	n/a
34	chr14:64319543-64319593	HRPEpiC	eye:	n/a
35	chr14:64319812-64319862	HCPEpiC	choroid plexus:	n/a
36	chr14:64319245-64319295	SAEC	small airway:	n/a
37	chr14:64319306-64319356	U87	brain:	n/a
38	chr14:64319306-64319356	HMEC	breast:	n/a
39	chr14:64319275-64319325	HCT-116	colon:	n/a
40	chr14:64320521-64320571	Caco-2	colon:	n/a
41	chr14:64319812-64319862	NH-A	brain:	n/a
42	chr14:64319275-64319325	GM12891	blood:	n/a
43	chr14:64319543-64319593	GM12891	blood:	n/a
44	chr14:64320049-64320099	T-47D	breast:	n/a
45	chr14:64319275-64319325	AoSMC	blood vessel:	n/a
46	chr14:64319543-64319593	K562	blood:	n/a
47	chr14:64319543-64319593	HRCEpiC	kidney:	n/a
48	chr14:64320521-64320571	HCM	heart:	n/a
49	chr14:64320118-64320168	HIPEpiC	eye:	n/a
50	chr14:64319306-64319356	NHDF-neo	bronchial:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:13044235..13044810-chr14:64320099..64320720,2	Hela-S3	cervix:
2	chr14:64319297..64319918-chr6:86352603..86353316,2	Hela-S3	cervix:
3	chr14:64319797..64321605-chr14:64466270..64468504,2	MCF-7	breast:
4	chr14:64318775..64319715-chr6:26156466..26157229,2	Hela-S3	cervix:
5	chr14:64319483..64322302-chr14:64328481..64332813,5	MCF-7	breast:
6	chr14:64319166..64320923-chr14:64328806..64331982,4	MCF-7	breast:
7	chr14:64319297..64320096-chr2:74425675..74426285,2	Hela-S3	cervix:
8	chr14:64319794..64321904-chr14:64361235..64363695,2	MCF-7	breast:

No data

Variant related genes	Relation type
SYNE2	TF binding region
ENSG00000202182	TF binding region
SYNE2	CpG island
ENSG00000202182	CpG island
ENSG00000054654	chromatin interactions
ENSG00000135316	chromatin interactions
ENSG00000013588	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000065911	chromatin interactions

Extended variants
information (count: 79 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:79 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147728622	chr14:64319224-64319225	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs541100581	chr14:64319281-64319282	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs553134434	chr14:64319352-64319353	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs572960421	chr14:64319391-64319392	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs12431956	chr14:64319425-64319426	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs373425120	chr14:64319441-64319442	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs575450222	chr14:64319449-64319450	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs149162800	chr14:64319471-64319472	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs564213890	chr14:64319472-64319473	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs532583878	chr14:64319480-64319481	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs545768638	chr14:64319522-64319523	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs559453520	chr14:64319531-64319532	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs528530467	chr14:64319595-64319596	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs548395099	chr14:64319624-64319625	Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs568600716	chr14:64319625-64319626	Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs531002235	chr14:64319630-64319631	Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs551305180	chr14:64319645-64319646	Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs571035920	chr14:64319688-64319689	Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs143315154	chr14:64319689-64319690	Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs552973060	chr14:64319711-64319712	Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs566597058	chr14:64319825-64319826	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs535493323	chr14:64319870-64319871	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs111348839	chr14:64319874-64319875	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs148287408	chr14:64319882-64319883	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs140452229	chr14:64319883-64319884	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs544071383	chr14:64319925-64319926	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs558059532	chr14:64319926-64319927	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs564771850	chr14:64319943-64319944	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs577498398	chr14:64319994-64319995	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs545809042	chr14:64319996-64319997	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs559293505	chr14:64319999-64320000	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs376457067	chr14:64320037-64320038	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs573011248	chr14:64320095-64320096	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs541961221	chr14:64320100-64320101	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs575073065	chr14:64320186-64320187	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs145527224	chr14:64320207-64320208	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs374272724	chr14:64320228-64320229	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs550881388	chr14:64320259-64320260	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs564818536	chr14:64320476-64320477	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs533642037	chr14:64320521-64320522	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs77692787	chr14:64320543-64320544	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs546623993	chr14:64320554-64320555	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs374608587	chr14:64320568-64320569	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs552251396	chr14:64320602-64320603	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs566432320	chr14:64320639-64320640	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs563084822	chr14:64320691-64320692	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs113116854	chr14:64320704-64320705	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs111872590	chr14:64320739-64320740	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs376534992	chr14:64320800-64320801	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs35131482	chr14:64320881-64320882	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Leukemia	18688285	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Autism	22543975	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64318800-64319400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
2	chr14:64318800-64319600	Active TSS	Fetal Lung	lung
3	chr14:64318800-64321000	Active TSS	HUES48 Cell Line	embryonic stem cell
4	chr14:64318800-64321200	Active TSS	H9 Cell Line	embryonic stem cell
5	chr14:64318800-64321400	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr14:64318800-64321800	Active TSS	Fetal Kidney	kidney
7	chr14:64318800-64322600	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr14:64319000-64319400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr14:64319000-64319400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr14:64319000-64319400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr14:64319000-64319400	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr14:64319000-64319400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
13	chr14:64319000-64319400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
14	chr14:64319000-64319400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
15	chr14:64319000-64319400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr14:64319000-64319400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr14:64319000-64319400	Flanking Active TSS	Brain Substantia Nigra	brain
18	chr14:64319000-64319400	Enhancers	Esophagus	oesophagus
19	chr14:64319000-64319400	Flanking Active TSS	Fetal Heart	heart
20	chr14:64319000-64319400	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
21	chr14:64319000-64319400	Flanking Active TSS	Fetal Stomach	stomach
22	chr14:64319000-64319400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
23	chr14:64319000-64319400	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr14:64319000-64319400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
25	chr14:64319000-64319400	Flanking Active TSS	Stomach Smooth Muscle	stomach
26	chr14:64319000-64319400	Flanking Active TSS	GM12878-XiMat	blood
27	chr14:64319000-64319400	Flanking Active TSS	Hela-S3	cervix
28	chr14:64319000-64319400	Flanking Bivalent TSS/Enh	HepG2	liver
29	chr14:64319000-64319400	Flanking Bivalent TSS/Enh	Osteobl	bone
30	chr14:64319000-64319600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
31	chr14:64319000-64319600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
32	chr14:64319000-64319600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr14:64319000-64319600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr14:64319000-64319600	Flanking Active TSS	Adipose Nuclei	Adipose
35	chr14:64319000-64319600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
36	chr14:64319000-64319600	Enhancers	Fetal Brain Male	brain
37	chr14:64319000-64319600	Flanking Active TSS	Dnd41	blood
38	chr14:64319000-64319600	Flanking Active TSS	NHEK	skin
39	chr14:64319000-64320800	Active TSS	Brain Hippocampus Middle	brain
40	chr14:64319000-64320800	Active TSS	Brain Inferior Temporal Lobe	brain
41	chr14:64319000-64320800	Active TSS	Colonic Mucosa	Colon
42	chr14:64319000-64321000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr14:64319000-64321000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr14:64319000-64321000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr14:64319000-64321000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr14:64319000-64321000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr14:64319000-64321000	Active TSS	Brain Anterior Caudate	brain
48	chr14:64319000-64321000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
49	chr14:64319000-64321000	Active TSS	Colon Smooth Muscle	Colon
50	chr14:64319000-64321000	Active TSS	Duodenum Mucosa	Duodenum

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