Variant report

Variant	esv3336600
Chromosome Location	chr5:114504203-114506901
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:531)
CpG islands
(count:244)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:531 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:114505309-114505674	HepG2	liver:	n/a	n/a
2	ATF2	chr5:114505270-114505723	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr5:114506375-114506464	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr5:114505176-114505883	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr5:114505230-114505877	A549	lung:	n/a	chr5:114505279-114505288 chr5:114505567-114505580 chr5:114505806-114505815
6	BHLHE40	chr5:114505122-114505876	GM12878	blood:	n/a	chr5:114505712-114505728
7	BHLHE40	chr5:114505180-114506131	HepG2	liver:	n/a	chr5:114505712-114505728 chr5:114505954-114505970
8	BHLHE40	chr5:114505096-114506073	K562	blood:	n/a	chr5:114505712-114505728 chr5:114505954-114505970
9	BHLHE40	chr5:114505207-114505553	A549	lung:	n/a	n/a
10	BRCA1	chr5:114505344-114505804	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr5:114505540-114505794	HepG2	liver:	n/a	n/a
12	BRCA1	chr5:114505470-114505715	H1-hESC	embryonic stem cell:	n/a	n/a
13	CBX3	chr5:114505295-114505999	K562	blood:	n/a	n/a
14	CCNT2	chr5:114505236-114506493	K562	blood:	n/a	n/a
15	CCNT2	chr5:114504747-114504971	K562	blood:	n/a	n/a
16	CEBPB	chr5:114505125-114505471	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr5:114505528-114505722	HepG2	liver:	n/a	n/a
18	CEBPB	chr5:114505060-114505310	HepG2	liver:	n/a	n/a
19	CEBPB	chr5:114506326-114506356	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr5:114504982-114505309	A549	lung:	n/a	n/a
21	CEBPB	chr5:114504965-114506085	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr5:114505011-114505309	K562	blood:	n/a	n/a
23	CHD1	chr5:114506656-114506726	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD1	chr5:114506020-114506135	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr5:114505105-114505505	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr5:114505381-114505822	HepG2	liver:	n/a	n/a
27	CHD2	chr5:114505536-114505822	GM12878	blood:	n/a	n/a
28	CHD2	chr5:114506137-114506255	HepG2	liver:	n/a	n/a
29	CHD2	chr5:114506520-114506546	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr5:114505327-114506096	K562	blood:	n/a	chr5:114505948-114505958
31	CHD2	chr5:114505374-114505886	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr5:114504684-114506334	Hela-S3	cervix:	n/a	chr5:114505948-114505958
33	CREB1	chr5:114505114-114506441	A549	lung:	n/a	n/a
34	CREB1	chr5:114505268-114506172	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr5:114505202-114506235	HepG2	liver:	n/a	n/a
36	CTBP2	chr5:114504745-114506603	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr5:114505515-114505688	GM19240	blood:	n/a	n/a
38	CTCF	chr5:114505568-114505699	LNCaP	prostate:	n/a	n/a
39	CTCF	chr5:114505500-114505650	HRE	kidney:	n/a	n/a
40	CTCF	chr5:114505500-114505650	HEK293	kidney:	n/a	n/a
41	CTCF	chr5:114505529-114505673	ProgFib	skin:	n/a	n/a
42	CTCF	chr5:114505580-114505730	HCT-116	colon:	n/a	n/a
43	CTCF	chr5:114505500-114505650	GM12868	blood:	n/a	n/a
44	CTCF	chr5:114505538-114505691	Lung_OC	lung:	n/a	n/a
45	CTCF	chr5:114505560-114505710	HAc	cerebellar:	n/a	n/a
46	CTCF	chr5:114505160-114505310	HCM	heart:	n/a	n/a
47	CTCF	chr5:114505511-114505687	MCF-7	breast:	n/a	n/a
48	CTCF	chr5:114505520-114505670	AG04449	skin:	n/a	n/a
49	CTCF	chr5:114505498-114505697	GM12878	blood:	n/a	n/a
50	CTCF	chr5:114505460-114505610	GM12873	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:114506309-114506359	LNCaP	prostate:	n/a
2	chr5:114506448-114506498	HRCEpiC	kidney:	n/a
3	chr5:114505766-114505816	HEEpiC	esophagus:	n/a
4	chr5:114504983-114505033	GM12878	blood:	n/a
5	chr5:114505766-114505816	HRCEpiC	kidney:	n/a
6	chr5:114504983-114505033	HCPEpiC	choroid plexus:	n/a
7	chr5:114505766-114505816	Hepatocyte	liver:	n/a
8	chr5:114506309-114506359	BE2_C	brain:	n/a
9	chr5:114504983-114505033	HAEpiC	amniotic membrane:	n/a
10	chr5:114506309-114506359	SK-N-SH_RA	brain:	n/a
11	chr5:114506309-114506359	SK-N-SH	brain:	n/a
12	chr5:114505766-114505816	GM12891	blood:	n/a
13	chr5:114505766-114505816	NHBE	bronchial:	n/a
14	chr5:114506448-114506498	NHBE	bronchial:	n/a
15	chr5:114506448-114506498	HRPEpiC	eye:	n/a
16	chr5:114505766-114505816	SK-N-MC	brain:	n/a
17	chr5:114506309-114506359	CMK	blood:	n/a
18	chr5:114504983-114505033	NH-A	brain:	n/a
19	chr5:114506309-114506359	HEEpiC	esophagus:	n/a
20	chr5:114505766-114505816	U87	brain:	n/a
21	chr5:114504983-114505033	NB4	blood:	n/a
22	chr5:114506309-114506359	HRCEpiC	kidney:	n/a
23	chr5:114506309-114506359	HCM	heart:	n/a
24	chr5:114504983-114505033	SK-N-SH_RA	brain:	n/a
25	chr5:114504983-114505033	AG04449	skin:	fetal
26	chr5:114506448-114506498	HEEpiC	esophagus:	n/a
27	chr5:114505766-114505816	ovcar-3	ovarian:	n/a
28	chr5:114505766-114505816	H1-hESC	embryonic stem cell:	embryo
29	chr5:114504983-114505033	HRE	kidney:	n/a
30	chr5:114505766-114505816	BJ	skin:	n/a
31	chr5:114506448-114506498	AG04449	skin:	fetal
32	chr5:114506448-114506498	HCT-116	colon:	n/a
33	chr5:114505766-114505816	SKMC	muscle:	n/a
34	chr5:114506448-114506498	PrEC	prostate:	n/a
35	chr5:114505766-114505816	PrEC	prostate:	n/a
36	chr5:114506448-114506498	PFSK-1	brain:	n/a
37	chr5:114505766-114505816	SK-N-SH_RA	brain:	n/a
38	chr5:114504983-114505033	GM12892	blood:	n/a
39	chr5:114506448-114506498	HAEpiC	amniotic membrane:	n/a
40	chr5:114504983-114505033	BE2_C	brain:	n/a
41	chr5:114505766-114505816	HIPEpiC	eye:	n/a
42	chr5:114504983-114505033	SKMC	muscle:	n/a
43	chr5:114504983-114505033	HRPEpiC	eye:	n/a
44	chr5:114506309-114506359	HepG2	liver:	n/a
45	chr5:114505766-114505816	SK-N-SH	brain:	n/a
46	chr5:114504983-114505033	CMK	blood:	n/a
47	chr5:114505766-114505816	Hela-S3	cervix:	n/a
48	chr5:114504983-114505033	AG10803	skin:	n/a
49	chr5:114505766-114505816	GM12878	blood:	n/a
50	chr5:114506448-114506498	AG09319	gingival:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:114505970..114507896-chr5:114509375..114511421,2	K562	blood:
2	chr5:114432281..114434501-chr5:114505854..114507519,2	MCF-7	breast:
3	chr3:48513994..48514495-chr5:114505101..114505601,2	NB4	blood:
4	chr5:114504108..114507715-chr5:114515140..114518807,4	MCF-7	breast:
5	chr5:114505745..114508021-chr5:114511446..114514175,2	K562	blood:
6	chr5:114504001..114505595-chr5:114509274..114511194,2	K562	blood:
7	chr5:114504319..114509129-chr5:114509356..114517256,16	MCF-7	breast:
8	chr5:114504828..114507303-chr5:114508620..114510973,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PGGT1B-7	chr5:114506803-114506919	NONHSAT103290

No data

Variant related genes	Relation type
TRIM36	TF binding region
TRIM36	CpG island
ENSG00000164054	chromatin interactions
ENSG00000152503	chromatin interactions

Extended variants
information (count: 110 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:110 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572533637	chr5:114504271-114504272	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs535102973	chr5:114504282-114504283	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs540767843	chr5:114504302-114504303	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs182199642	chr5:114504304-114504305	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs545952450	chr5:114504318-114504319	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs141366017	chr5:114504362-114504363	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs187741611	chr5:114504403-114504404	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs577841911	chr5:114504405-114504406	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs371957853	chr5:114504422-114504423	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs540547020	chr5:114504451-114504452	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs150214468	chr5:114504496-114504497	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs529268517	chr5:114504501-114504502	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs138844784	chr5:114504522-114504523	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs562926668	chr5:114504556-114504557	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs192735550	chr5:114504572-114504573	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs531883294	chr5:114504578-114504579	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs973	chr5:114504589-114504590	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs142912600	chr5:114504592-114504593	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs188357598	chr5:114504602-114504603	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs534206021	chr5:114504607-114504608	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs374399219	chr5:114504648-114504649	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs376907675	chr5:114504709-114504710	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs547657050	chr5:114504727-114504728	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs528454071	chr5:114504777-114504778	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs567627633	chr5:114504803-114504804	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs535038215	chr5:114504823-114504824	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs149349204	chr5:114504824-114504825	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs574983954	chr5:114504827-114504828	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs113343998	chr5:114504847-114504848	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs7724952	chr5:114504855-114504856	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs562041283	chr5:114504892-114504893	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs577736085	chr5:114504912-114504913	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs114724385	chr5:114504947-114504948	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs529498978	chr5:114505002-114505003	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs554070565	chr5:114505035-114505036	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs573989924	chr5:114505049-114505050	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs184633953	chr5:114505091-114505092	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs562912618	chr5:114505108-114505109	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs531697911	chr5:114505215-114505216	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs189448314	chr5:114505218-114505219	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs545513844	chr5:114505226-114505227	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs565257401	chr5:114505234-114505235	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs367572891	chr5:114505238-114505239	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs555971638	chr5:114505251-114505252	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs569320600	chr5:114505252-114505253	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs527852354	chr5:114505253-114505254	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs547588013	chr5:114505278-114505279	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs371799441	chr5:114505282-114505283	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs375839245	chr5:114505324-114505325	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs530365354	chr5:114505378-114505379	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:477 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114501400-114504800	Weak transcription	Gastric	stomach
2	chr5:114502800-114504400	Weak transcription	Colonic Mucosa	Colon
3	chr5:114502800-114504800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:114503000-114504600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr5:114503000-114504600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr5:114503000-114504800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr5:114503400-114504600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr5:114503600-114504400	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr5:114503800-114504400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr5:114504000-114504800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
11	chr5:114504000-114505000	Active TSS	Fetal Brain Female	brain
12	chr5:114504000-114505400	Active TSS	Fetal Brain Male	brain
13	chr5:114504000-114506200	Active TSS	Rectal Mucosa Donor 29	rectum
14	chr5:114504200-114504400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr5:114504200-114504400	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:114504200-114504400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
17	chr5:114504200-114504400	Active TSS	Cortex derived primary cultured neurospheres	brain
18	chr5:114504200-114504400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr5:114504200-114504400	Enhancers	Brain Anterior Caudate	brain
20	chr5:114504200-114504400	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr5:114504200-114504400	Enhancers	HMEC	breast
22	chr5:114504200-114504600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
23	chr5:114504200-114504600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
24	chr5:114504200-114504600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr5:114504200-114504600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr5:114504200-114504600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
27	chr5:114504200-114504600	Flanking Active TSS	Duodenum Mucosa	Duodenum
28	chr5:114504200-114504600	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
29	chr5:114504200-114504600	Bivalent Enhancer	Fetal Heart	heart
30	chr5:114504200-114504800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
31	chr5:114504200-114504800	Active TSS	Brain Germinal Matrix	brain
32	chr5:114504200-114504800	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr5:114504200-114504800	Flanking Active TSS	Hela-S3	cervix
34	chr5:114504200-114505000	Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr5:114504200-114505200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
36	chr5:114504200-114505200	Active TSS	Right Atrium	heart
37	chr5:114504200-114506000	Active TSS	NH-A	brain
38	chr5:114504200-114506200	Active TSS	Brain Cingulate Gyrus	brain
39	chr5:114504200-114506600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr5:114504200-114506600	Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr5:114504200-114506600	Active TSS	Brain Angular Gyrus	brain
42	chr5:114504200-114506600	Active TSS	HSMMtube	muscle
43	chr5:114504200-114506800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr5:114504200-114507000	Active TSS	Brain Inferior Temporal Lobe	brain
45	chr5:114504200-114507400	Active TSS	Rectal Mucosa Donor 31	rectum
46	chr5:114504400-114504600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
47	chr5:114504400-114504600	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr5:114504400-114504600	Bivalent Enhancer	Primary T cells from cord blood	blood
49	chr5:114504400-114504600	Enhancers	Adipose Nuclei	Adipose
50	chr5:114504400-114504600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet

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