Variant report

Variant	nsv462586
Chromosome Location	chr5:180119918-180213878
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:636)
CpG islands
(count:429)
Chromatin interactive
region (count:42)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:636 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:180144959-180145359	GM12878	blood:	n/a	n/a
2	ATF2	chr5:180212570-180213141	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr5:180212679-180213244	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr5:180145040-180145312	GM12878	blood:	n/a	chr5:180145207-180145218
5	BATF	chr5:180169789-180169977	GM12878	blood:	n/a	n/a
6	BATF	chr5:180145061-180145379	GM12878	blood:	n/a	chr5:180145207-180145218
7	BCL11A	chr5:180145100-180145299	GM12878	blood:	n/a	chr5:180145235-180145244
8	BCL11A	chr5:180145000-180145348	GM12878	blood:	n/a	chr5:180145235-180145244
9	CBX3	chr5:180198844-180199194	K562	blood:	n/a	n/a
10	CBX3	chr5:180127492-180127736	K562	blood:	n/a	n/a
11	CBX3	chr5:180208858-180209504	K562	blood:	n/a	n/a
12	CBX3	chr5:180208965-180209392	K562	blood:	n/a	n/a
13	CBX3	chr5:180198766-180199290	K562	blood:	n/a	n/a
14	CEBPB	chr5:180131341-180131657	K562	blood:	n/a	n/a
15	CEBPB	chr5:180208882-180209430	K562	blood:	n/a	n/a
16	CEBPB	chr5:180209005-180209250	K562	blood:	n/a	n/a
17	CEBPD	chr5:180208780-180209396	K562	blood:	n/a	n/a
18	CEBPD	chr5:180131384-180131803	K562	blood:	n/a	n/a
19	CEBPD	chr5:180208777-180209303	K562	blood:	n/a	n/a
20	CREB1	chr5:180144917-180145413	GM12878	blood:	n/a	n/a
21	CREB1	chr5:180144836-180145451	GM12878	blood:	n/a	n/a
22	CTCF	chr5:180211620-180211770	Hela-S3	cervix:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
23	CTCF	chr5:180145820-180145970	BE2_C	brain:	n/a	n/a
24	CTCF	chr5:180211555-180211820	GM13977	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
25	CTCF	chr5:180145820-180145970	HEEpiC	esophagus:	n/a	n/a
26	CTCF	chr5:180145794-180146044	LNCaP	prostate:	n/a	n/a
27	CTCF	chr5:180145505-180145624	A549	lung:	n/a	n/a
28	CTCF	chr5:180145864-180145997	GM19240	blood:	n/a	n/a
29	CTCF	chr5:180145860-180146010	GM12869	blood:	n/a	n/a
30	CTCF	chr5:180145460-180145610	HRE	kidney:	n/a	n/a
31	CTCF	chr5:180146520-180146670	HRE	kidney:	n/a	n/a
32	CTCF	chr5:180145860-180146010	HCM	heart:	n/a	n/a
33	CTCF	chr5:180145820-180145970	RPTEC	kidney:	n/a	n/a
34	CTCF	chr5:180145820-180145970	SAEC	small airway:	n/a	n/a
35	CTCF	chr5:180143280-180143430	GM12872	blood:	n/a	n/a
36	CTCF	chr5:180211560-180211710	AG04450	lung:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
37	CTCF	chr5:180145820-180145970	GM12872	blood:	n/a	n/a
38	CTCF	chr5:180146480-180146630	HAc	cerebellar:	n/a	n/a
39	CTCF	chr5:180211620-180211770	HMEC	breast:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
40	CTCF	chr5:180211560-180211710	HFF-Myc	foreskin:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
41	CTCF	chr5:180211620-180211770	AoAF	blood vessel:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
42	CTCF	chr5:180211600-180211750	GM12874	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
43	CTCF	chr5:180145858-180145965	GM19239	blood:	n/a	n/a
44	CTCF	chr5:180146238-180146280	GM12892	blood:	n/a	n/a
45	CTCF	chr5:180145632-180146378	SK-N-SH	brain:	n/a	n/a
46	CTCF	chr5:180211620-180211770	SK-N-SH_RA	brain:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
47	CTCF	chr5:180211577-180211804	ProgFib	skin:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
48	CTCF	chr5:180211556-180211829	HepG2	liver:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
49	CTCF	chr5:180211542-180211821	A549	lung:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
50	CTCF	chr5:180145840-180145990	NHDF-neo	bronchial:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:180167132-180167182	Hepatocyte	liver:	n/a
2	chr5:180167132-180167182	HIPEpiC	eye:	n/a
3	chr5:180167132-180167182	Hepatocyte	liver:	n/a
4	chr5:180167132-180167182	HIPEpiC	eye:	n/a
5	chr5:180167566-180167616	PANC-1	pancreas:	n/a
6	chr5:180167965-180168015	SK-N-SH	brain:	n/a
7	chr5:180166694-180166744	PFSK-1	brain:	n/a
8	chr5:180213189-180213239	MCF-7	breast:	n/a
9	chr5:180167724-180167774	PANC-1	pancreas:	n/a
10	chr5:180167132-180167182	HPAEpiC	pulmonary alveolar:	n/a
11	chr5:180166492-180166542	HIPEpiC	eye:	n/a
12	chr5:180167724-180167774	Jurkat	blood:	n/a
13	chr5:180167566-180167616	HIPEpiC	eye:	n/a
14	chr5:180167566-180167616	HUVEC	blood vessel:	n/a
15	chr5:180166694-180166744	HMEC	breast:	n/a
16	chr5:180166694-180166744	SK-N-SH	brain:	n/a
17	chr5:180166492-180166542	HCPEpiC	choroid plexus:	n/a
18	chr5:180213189-180213239	GM12891	blood:	n/a
19	chr5:180167566-180167616	HRPEpiC	eye:	n/a
20	chr5:180167132-180167182	Jurkat	blood:	n/a
21	chr5:180167724-180167774	LNCaP	prostate:	n/a
22	chr5:180213189-180213239	RPTEC	kidney:	n/a
23	chr5:180213189-180213239	HPAEpiC	pulmonary alveolar:	n/a
24	chr5:180167965-180168015	MCF10A-Er-Src	breast:	n/a
25	chr5:180167132-180167182	Hela-S3	cervix:	n/a
26	chr5:180166694-180166744	Hela-S3	cervix:	n/a
27	chr5:180167132-180167182	PANC-1	pancreas:	n/a
28	chr5:180167965-180168015	U87	brain:	n/a
29	chr5:180166492-180166542	PrEC	prostate:	n/a
30	chr5:180167965-180168015	HUVEC	blood vessel:	n/a
31	chr5:180167965-180168015	HL-60	blood:	n/a
32	chr5:180213189-180213239	PrEC	prostate:	n/a
33	chr5:180167566-180167616	HCF	heart:	n/a
34	chr5:180166694-180166744	NB4	blood:	n/a
35	chr5:180213189-180213239	ProgFib	skin:	n/a
36	chr5:180167965-180168015	Jurkat	blood:	n/a
37	chr5:180167724-180167774	NH-A	brain:	n/a
38	chr5:180213189-180213239	BE2_C	brain:	n/a
39	chr5:180167724-180167774	ProgFib	skin:	n/a
40	chr5:180166694-180166744	HNPCEpiC	eye:	n/a
41	chr5:180213189-180213239	MCF10A-Er-Src	breast:	n/a
42	chr5:180167132-180167182	PFSK-1	brain:	n/a
43	chr5:180167965-180168015	NH-A	brain:	n/a
44	chr5:180213189-180213239	NH-A	brain:	n/a
45	chr5:180167965-180168015	AG04449	skin:	fetal
46	chr5:180167132-180167182	T-47D	breast:	n/a
47	chr5:180213189-180213239	HepG2	liver:	n/a
48	chr5:180167724-180167774	HCM	heart:	n/a
49	chr5:180167132-180167182	HCM	heart:	n/a
50	chr5:180167965-180168015	PrEC	prostate:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:180168086..180169925-chr5:180190599..180192805,2	K562	blood:
2	chr5:180037911..180038640-chr5:180145288..180145999,2	MCF-7	breast:
3	chr5:180136617..180138276-chr5:180153652..180155749,2	K562	blood:
4	chr5:180209019..180210957-chr5:180453882..180456380,2	K562	blood:
5	chr5:180172009..180174376-chr5:180240608..180243076,2	MCF-7	breast:
6	chr5:180170663..180173512-chr5:180175093..180176860,2	K562	blood:
7	chr5:180158275..180159905-chr5:180163258..180165205,2	K562	blood:
8	chr5:180153993..180156519-chr5:180159947..180161759,2	K562	blood:
9	chr5:180130605..180132994-chr5:180134010..180136773,2	MCF-7	breast:
10	chr5:180171538..180174150-chr5:180179388..180180987,2	K562	blood:
11	chr5:180210430..180214631-chr5:180286463..180290673,6	MCF-7	breast:
12	chr5:180208930..180211085-chr5:180226767..180229407,2	K562	blood:
13	chr5:180130605..180132994-chr5:180134010..180136773,2	MCF-7	breast:
14	chr5:180211185..180212156-chr5:180225940..180226892,9	MCF-7	breast:
15	chr5:180208714..180211702-chr5:180212096..180213803,2	K562	blood:
16	chr5:180207628..180210924-chr5:180228309..180230947,5	MCF-7	breast:
17	chr5:179919075..179921338-chr5:180210769..180213087,2	MCF-7	breast:
18	chr5:180170663..180173512-chr5:180175093..180176860,2	K562	blood:
19	chr5:180168086..180169925-chr5:180190599..180192805,2	K562	blood:
20	chr5:180097643..180098351-chr5:180145367..180146387,3	MCF-7	breast:
21	chr5:180154735..180156600-chr5:180159240..180161653,2	MCF-7	breast:
22	chr5:180207548..180210211-chr5:180589188..180591545,3	K562	blood:
23	chr5:180136617..180138276-chr5:180153652..180155749,2	K562	blood:
24	chr5:180211281..180211887-chr5:180586366..180586939,2	MCF-7	breast:
25	chr5:180146148..180147851-chr5:180235768..180238086,2	K562	blood:
26	chr5:180143140..180144948-chr5:180229622..180231793,2	K562	blood:
27	chr5:180202321..180205166-chr5:180643152..180645917,2	K562	blood:
28	chr5:180168390..180170515-chr5:180204872..180207367,2	K562	blood:
29	chr5:180210073..180212750-chr5:180649135..180651698,2	MCF-7	breast:
30	chr5:180208714..180211260-chr5:180212096..180214924,3	K562	blood:
31	chr5:180153993..180156519-chr5:180159947..180161759,2	K562	blood:
32	chr5:180212092..180214294-chr5:180453988..180456472,2	K562	blood:
33	chr5:180202113..180204208-chr5:180208493..180210882,2	K562	blood:
34	chr5:180171538..180174150-chr5:180179388..180180987,2	K562	blood:
35	chr5:180147687..180149481-chr5:180151717..180153867,2	K562	blood:
36	chr5:180202113..180204208-chr5:180208493..180210882,2	K562	blood:
37	chr5:180211375..180212214-chr5:180226180..180226854,2	MCF-7	breast:
38	chr5:180208714..180211702-chr5:180212096..180213803,2	K562	blood:
39	chr5:180168390..180170515-chr5:180204872..180207367,2	K562	blood:
40	chr5:180147687..180149481-chr5:180151717..180153867,2	K562	blood:
41	chr5:180211640..180213961-chr5:180214094..180219248,5	K562	blood:
42	chr5:180158275..180159905-chr5:180163258..180165205,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTNL8-8	chr5:180192279-180192466	ucscGeneNc_uc003mmk_2
2	lnc-BTNL8-8	chr5:180190563-180190835	ucscGeneNc_uc003mmk_2
3	lnc-OR2Y1-1	chr5:180155280-180155484	expReg_chr5_11028_-
4	lnc-OR2Y1-2	chr5:180189565-180191201	ucscGeneNc_uc003mmj_1
5	lnc-BTNL8-8	chr5:180193918-180195284	ucscGeneNc_uc003mmk_2

No data

Variant related genes	Relation type
RNU1-17P	TF binding region
OR2Y1	TF binding region
OR2AI1P	TF binding region
RNU1-17P	CpG island
OR2Y1	CpG island
OR2AI1P	CpG island
ENSG00000199892	chromatin interactions
ENSG00000131446	chromatin interactions
ENSG00000260841	chromatin interactions
ENSG00000264732	chromatin interactions
ENSG00000146063	chromatin interactions
ENSG00000196670	chromatin interactions

Extended variants
information (count: 2169 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:2169 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10055973	chr5:180119918-180119919	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576179827	chr5:180119920-180119921	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs60350100	chr5:180119948-180119949	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs11738161	chr5:180120010-180120011	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs13188129	chr5:180120044-180120045	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs541059085	chr5:180120045-180120046	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs10071630	chr5:180120068-180120069	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs57118750	chr5:180120085-180120086	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs549853785	chr5:180120112-180120113	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs563739314	chr5:180120122-180120123	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs529441023	chr5:180120140-180120141	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs11738216	chr5:180120149-180120150	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs184869333	chr5:180120174-180120175	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs78056572	chr5:180120175-180120176	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs114918368	chr5:180120186-180120187	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs7731780	chr5:180120192-180120193	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs539585621	chr5:180120197-180120198	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs189249588	chr5:180120200-180120201	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs7341096	chr5:180120226-180120227	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs569756112	chr5:180120246-180120247	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs535601071	chr5:180120331-180120332	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs375448730	chr5:180120369-180120370	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs561183577	chr5:180120384-180120385	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs555254054	chr5:180120385-180120386	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs572330670	chr5:180120399-180120400	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs540920263	chr5:180120400-180120401	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs140602478	chr5:180120415-180120416	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs76824484	chr5:180120507-180120508	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs6601136	chr5:180120528-180120529	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs563773490	chr5:180120553-180120554	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs531925787	chr5:180120569-180120570	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs116564976	chr5:180120573-180120574	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs377244967	chr5:180120598-180120599	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs543241792	chr5:180120662-180120663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559671015	chr5:180120699-180120700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528841171	chr5:180120723-180120724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs10073529	chr5:180120738-180120739	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs570475017	chr5:180120795-180120796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181525395	chr5:180120822-180120823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532912158	chr5:180120824-180120825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568116401	chr5:180120871-180120872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549925121	chr5:180120894-180120895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533970602	chr5:180120981-180120982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs72824470	chr5:180121017-180121018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs376164125	chr5:180121023-180121024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs546465988	chr5:180121127-180121128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565725008	chr5:180121148-180121149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528432820	chr5:180121300-180121301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534613077	chr5:180121301-180121302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs10073887	chr5:180121337-180121338	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:109)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	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
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
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	17440070	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:180116600-180120000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:180116600-180130800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr5:180117000-180120000	Enhancers	Primary T killer memory cells from peripheral blood	blood
4	chr5:180117000-180120600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr5:180117000-180120800	Enhancers	Fetal Thymus	thymus
6	chr5:180117200-180120400	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr5:180117200-180120400	Enhancers	Thymus	Thymus
8	chr5:180117200-180121400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr5:180117400-180120600	Enhancers	Primary T cells from cord blood	blood
10	chr5:180117400-180120600	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr5:180119000-180120000	Weak transcription	Dnd41	blood
12	chr5:180119200-180120200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr5:180120000-180120200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr5:180120000-180120200	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr5:180120000-180120200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr5:180120000-180120200	Enhancers	Pancreas	Pancrea
17	chr5:180120000-180120200	Enhancers	Dnd41	blood
18	chr5:180120000-180120600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
19	chr5:180125800-180126400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr5:180126200-180127000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr5:180126200-180127200	Enhancers	H1 Cell Line	embryonic stem cell
22	chr5:180127200-180134800	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr5:180130800-180131600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr5:180131000-180131600	Enhancers	K562	blood
25	chr5:180131200-180131400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr5:180131200-180131600	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr5:180131200-180131600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr5:180131400-180131800	Enhancers	A549	lung
29	chr5:180131600-180134800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr5:180131600-180134800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr5:180131600-180135000	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr5:180134800-180135200	Enhancers	H1 Cell Line	embryonic stem cell
33	chr5:180134800-180135200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr5:180134800-180137200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr5:180134800-180138000	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr5:180135000-180135200	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr5:180135200-180135600	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr5:180135200-180137200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr5:180135200-180137200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr5:180135200-180137400	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr5:180135600-180137400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr5:180136000-180136200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr5:180136200-180138200	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr5:180136400-180137400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr5:180137200-180137400	Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr5:180137200-180138000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
47	chr5:180137200-180138600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr5:180137400-180137600	Enhancers	H1 Cell Line	embryonic stem cell
49	chr5:180137400-180137600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr5:180137400-180137800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell

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