Variant report

Variant	esv3341450
Chromosome Location	chr14:64318649-64321797
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:559)
CpG islands
(count:549)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:559 , 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	chr14:64320113-64320436	GM12878	blood:	n/a	chr14:64320182-64320198
3	BHLHE40	chr14:64320253-64320376	K562	blood:	n/a	n/a
4	BHLHE40	chr14:64320179-64320341	HepG2	liver:	n/a	chr14:64320182-64320198
5	BHLHE40	chr14:64320654-64320953	GM12878	blood:	n/a	n/a
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	chr14:64320622-64320926	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr14:64320750-64320938	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr14:64319571-64319813	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	chr14:64320146-64320354	GM12878	blood:	n/a	n/a
14	CHD1	chr14:64320555-64321411	GM12878	blood:	n/a	n/a
15	CHD2	chr14:64319487-64319824	Hela-S3	cervix:	n/a	chr14:64319776-64319783 chr14:64319670-64319680
16	CHD2	chr14:64320959-64320976	GM12878	blood:	n/a	n/a
17	CHD2	chr14:64320641-64320850	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr14:64320775-64320807	HepG2	liver:	n/a	n/a
19	CHD2	chr14:64320055-64320347	Hela-S3	cervix:	n/a	n/a
20	CREB1	chr14:64319426-64319954	A549	lung:	n/a	n/a
21	CREB1	chr14:64320172-64320390	A549	lung:	n/a	n/a
22	CREB1	chr14:64319984-64320511	A549	lung:	n/a	n/a
23	CTBP2	chr14:64319088-64319839	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr14:64319200-64319350	HAc	cerebellar:	n/a	n/a
25	CTCF	chr14:64320040-64320190	HEEpiC	esophagus:	n/a	chr14:64320111-64320124
26	CTCF	chr14:64319443-64319762	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr14:64319542-64319707	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr14:64320620-64320770	GM12870	blood:	n/a	n/a
29	CTCF	chr14:64320054-64320155	ProgFib	skin:	n/a	chr14:64320111-64320124
30	CTCF	chr14:64319560-64319710	RPTEC	kidney:	n/a	n/a
31	CTCF	chr14:64320600-64320750	GM12873	blood:	n/a	n/a
32	CTCF	chr14:64319545-64319709	MCF-7	breast:	n/a	n/a
33	CTCF	chr14:64319620-64319770	HFF	foreskin:	n/a	n/a
34	CTCF	chr14:64319540-64319690	AG04449	skin:	n/a	n/a
35	CTCF	chr14:64320000-64320150	GM12872	blood:	n/a	chr14:64320111-64320124
36	CTCF	chr14:64319600-64319750	GM12865	blood:	n/a	n/a
37	CTCF	chr14:64320023-64320215	Spleen_OC	spleen:	n/a	chr14:64320111-64320124
38	CTCF	chr14:64320258-64320260	GM19240	blood:	n/a	n/a
39	CTCF	chr14:64319400-64319550	GM12872	blood:	n/a	n/a
40	CTCF	chr14:64319580-64319730	AG09319	gingival:	n/a	n/a
41	CTCF	chr14:64320036-64320190	GM10248	blood:	n/a	chr14:64320111-64320124
42	CTCF	chr14:64319960-64320110	GM12873	blood:	n/a	n/a
43	CTCF	chr14:64320040-64320190	GM12873	blood:	n/a	chr14:64320111-64320124
44	CTCF	chr14:64320008-64320207	MCF-7	breast:	n/a	chr14:64320111-64320124
45	CTCF	chr14:64319980-64320130	HRE	kidney:	n/a	chr14:64320111-64320124
46	CTCF	chr14:64320041-64320181	A549	lung:	n/a	chr14:64320111-64320124
47	CTCF	chr14:64319540-64319690	HepG2	liver:	n/a	n/a
48	CTCF	chr14:64319535-64319709	LNCaP	prostate:	n/a	n/a
49	CTCF	chr14:64320040-64320190	GM12870	blood:	n/a	chr14:64320111-64320124
50	CTCF	chr14:64319980-64320130	HA-sp	spinal cord:	n/a	chr14:64320111-64320124

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:64319089-64319139	HCT-116	colon:	n/a
2	chr14:64319543-64319593	AG04449	skin:	fetal
3	chr14:64319089-64319139	H1-hESC	embryonic stem cell:	embryo
4	chr14:64320118-64320168	AG04449	skin:	fetal
5	chr14:64319275-64319325	A549	lung:	n/a
6	chr14:64319245-64319295	SK-N-SH_RA	brain:	n/a
7	chr14:64320118-64320168	NT2-D1	testis:	n/a
8	chr14:64320049-64320099	AoSMC	blood vessel:	n/a
9	chr14:64319089-64319139	BE2_C	brain:	n/a
10	chr14:64319245-64319295	PANC-1	pancreas:	n/a
11	chr14:64319089-64319139	HUVEC	blood vessel:	n/a
12	chr14:64320049-64320099	ProgFib	skin:	n/a
13	chr14:64320049-64320099	AG04450	lung:	fetal
14	chr14:64319543-64319593	Jurkat	blood:	n/a
15	chr14:64319275-64319325	Hepatocyte	liver:	n/a
16	chr14:64319543-64319593	SK-N-SH_RA	brain:	n/a
17	chr14:64319089-64319139	HEEpiC	esophagus:	n/a
18	chr14:64319543-64319593	AG09309	skin:	n/a
19	chr14:64319812-64319862	K562	blood:	n/a
20	chr14:64319543-64319593	PrEC	prostate:	n/a
21	chr14:64320049-64320099	U87	brain:	n/a
22	chr14:64319089-64319139	HPAEpiC	pulmonary alveolar:	n/a
23	chr14:64319089-64319139	HAEpiC	amniotic membrane:	n/a
24	chr14:64319245-64319295	MCF10A-Er-Src	breast:	n/a
25	chr14:64319245-64319295	K562	blood:	n/a
26	chr14:64320118-64320168	GM12891	blood:	n/a
27	chr14:64319245-64319295	HMEC	breast:	n/a
28	chr14:64319306-64319356	T-47D	breast:	n/a
29	chr14:64319245-64319295	GM06990	blood:	n/a
30	chr14:64320521-64320571	A549	lung:	n/a
31	chr14:64320521-64320571	NT2-D1	testis:	n/a
32	chr14:64319245-64319295	BJ	skin:	n/a
33	chr14:64320118-64320168	ovcar-3	ovarian:	n/a
34	chr14:64319306-64319356	HNPCEpiC	eye:	n/a
35	chr14:64320118-64320168	SK-N-SH_RA	brain:	n/a
36	chr14:64319245-64319295	GM12878	blood:	n/a
37	chr14:64320118-64320168	BE2_C	brain:	n/a
38	chr14:64320049-64320099	MCF-7	breast:	n/a
39	chr14:64319812-64319862	ovcar-3	ovarian:	n/a
40	chr14:64319089-64319139	AG09309	skin:	n/a
41	chr14:64319812-64319862	PANC-1	pancreas:	n/a
42	chr14:64320049-64320099	T-47D	breast:	n/a
43	chr14:64320049-64320099	SK-N-SH_RA	brain:	n/a
44	chr14:64319812-64319862	GM12878	blood:	n/a
45	chr14:64319543-64319593	IMR90	lung:	fetal
46	chr14:64319089-64319139	PrEC	prostate:	n/a
47	chr14:64319245-64319295	HNPCEpiC	eye:	n/a
48	chr14:64319306-64319356	MCF10A-Er-Src	breast:	n/a
49	chr14:64319275-64319325	PANC-1	pancreas:	n/a
50	chr14:64320521-64320571	NH-A	brain:	n/a

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

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

No data

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

Extended variants
information (count: 98 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:98 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575299673	chr14:64318694-64318695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs577780907	chr14:64318704-64318705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112225460	chr14:64318734-64318735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368330888	chr14:64318739-64318740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375600922	chr14:64318777-64318778	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs530352330	chr14:64318779-64318780	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs7161586	chr14:64318899-64318900	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs558704308	chr14:64318983-64318984	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs7144370	chr14:64319033-64319034	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs557919824	chr14:64319052-64319053	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs528686933	chr14:64319071-64319072	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs545447200	chr14:64319080-64319081	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs192552824	chr14:64319091-64319092	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs568674613	chr14:64319119-64319120	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs376795691	chr14:64319128-64319129	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs537702987	chr14:64319129-64319130	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs376893017	chr14:64319159-64319160	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs184366205	chr14:64319166-64319167	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs570468858	chr14:64319185-64319186	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	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
32	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
33	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
34	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
35	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
36	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
37	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
38	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
39	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
40	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
41	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
42	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
43	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
44	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
45	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
46	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
47	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
48	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
49	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
50	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

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:495 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64312800-64319200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr14:64315600-64319000	Weak transcription	Left Ventricle	heart
3	chr14:64316000-64318800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr14:64316000-64319000	Weak transcription	HUVEC	blood vessel
5	chr14:64316200-64319200	Weak transcription	Stomach Mucosa	stomach
6	chr14:64316600-64318800	Weak transcription	Fetal Heart	heart
7	chr14:64316600-64319000	Weak transcription	Adipose Nuclei	Adipose
8	chr14:64316600-64319000	Weak transcription	Ovary	ovary
9	chr14:64317200-64319000	Weak transcription	Right Ventricle	heart
10	chr14:64318800-64319000	Flanking Active TSS	H1 Cell Line	embryonic stem cell
11	chr14:64318800-64319000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
12	chr14:64318800-64319000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
13	chr14:64318800-64319000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr14:64318800-64319000	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr14:64318800-64319000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr14:64318800-64319000	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr14:64318800-64319000	Enhancers	Brain Substantia Nigra	brain
18	chr14:64318800-64319000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr14:64318800-64319000	Enhancers	Fetal Heart	heart
20	chr14:64318800-64319000	Enhancers	Fetal Stomach	stomach
21	chr14:64318800-64319000	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr14:64318800-64319000	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr14:64318800-64319000	Enhancers	Stomach Smooth Muscle	stomach
24	chr14:64318800-64319000	Enhancers	Dnd41	blood
25	chr14:64318800-64319000	Enhancers	GM12878-XiMat	blood
26	chr14:64318800-64319000	Enhancers	Hela-S3	cervix
27	chr14:64318800-64319000	Enhancers	NHEK	skin
28	chr14:64318800-64319200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
29	chr14:64318800-64319200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
30	chr14:64318800-64319400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
31	chr14:64318800-64319600	Active TSS	Fetal Lung	lung
32	chr14:64318800-64321000	Active TSS	HUES48 Cell Line	embryonic stem cell
33	chr14:64318800-64321200	Active TSS	H9 Cell Line	embryonic stem cell
34	chr14:64318800-64321400	Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr14:64318800-64321800	Active TSS	Fetal Kidney	kidney
36	chr14:64318800-64322600	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr14:64319000-64319200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
38	chr14:64319000-64319200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr14:64319000-64319200	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr14:64319000-64319200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
41	chr14:64319000-64319200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
42	chr14:64319000-64319200	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
43	chr14:64319000-64319200	Enhancers	Primary B cells from peripheral blood	blood
44	chr14:64319000-64319200	Enhancers	Primary T cells fromperipheralblood	blood
45	chr14:64319000-64319200	Enhancers	Primary hematopoietic stem cells	blood
46	chr14:64319000-64319200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
47	chr14:64319000-64319200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr14:64319000-64319200	Enhancers	Primary T helper naive cells from peripheral blood	blood
49	chr14:64319000-64319200	Enhancers	Primary T helper cells PMA-I stimulated	--
50	chr14:64319000-64319200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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