Variant report

Variant	nsv462387
Chromosome Location	chr5:112053911-112124369
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:915)
CpG islands
(count:1038)
Chromatin interactive
region (count:80)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:112075270-112075431	K562	blood:	n/a	n/a
2	ARID3A	chr5:112093343-112093652	K562	blood:	n/a	n/a
3	ARID3A	chr5:112074488-112075036	K562	blood:	n/a	n/a
4	ARID3A	chr5:112078257-112078771	K562	blood:	n/a	n/a
5	ARID3A	chr5:112069769-112070489	K562	blood:	n/a	n/a
6	ATF1	chr5:112078087-112078543	K562	blood:	n/a	n/a
7	ATF3	chr5:112073329-112073660	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr5:112073351-112073777	K562	blood:	n/a	chr5:112073766-112073775 chr5:112073754-112073774
9	ATF3	chr5:112073356-112073674	K562	blood:	n/a	n/a
10	ATF3	chr5:112073300-112073784	GM12878	blood:	n/a	chr5:112073766-112073775 chr5:112073754-112073774
11	ATF3	chr5:112073445-112073652	GM12878	blood:	n/a	n/a
12	ATF3	chr5:112073264-112073762	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr5:112078181-112078413	K562	blood:	n/a	n/a
14	BACH1	chr5:112073789-112073897	K562	blood:	n/a	n/a
15	BACH1	chr5:112098083-112098175	K562	blood:	n/a	n/a
16	BACH1	chr5:112078317-112078667	K562	blood:	n/a	n/a
17	BHLHE40	chr5:112078050-112078722	K562	blood:	n/a	n/a
18	BHLHE40	chr5:112060696-112060975	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:112073382-112073807	HepG2	liver:	n/a	chr5:112073534-112073543 chr5:112073532-112073545 chr5:112073535-112073544 chr5:112073534-112073543 chr5:112073528-112073549
20	BHLHE40	chr5:112073172-112074409	K562	blood:	n/a	chr5:112073534-112073543 chr5:112073532-112073545 chr5:112073535-112073544 chr5:112073534-112073543 chr5:112073528-112073549
21	BHLHE40	chr5:112073228-112074123	GM12878	blood:	n/a	chr5:112073534-112073543 chr5:112073532-112073545 chr5:112073535-112073544 chr5:112073534-112073543 chr5:112073528-112073549
22	BRCA1	chr5:112093416-112093570	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr5:112073070-112073664	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr5:112073397-112073398	GM12878	blood:	n/a	n/a
25	BRCA1	chr5:112073177-112073323	H1-hESC	embryonic stem cell:	n/a	n/a
26	CBX3	chr5:112078032-112078532	K562	blood:	n/a	n/a
27	CBX3	chr5:112073138-112074438	K562	blood:	n/a	n/a
28	CBX3	chr5:112061856-112062225	K562	blood:	n/a	n/a
29	CCNT2	chr5:112073239-112074084	K562	blood:	n/a	chr5:112073766-112073775 chr5:112073841-112073850 chr5:112073659-112073668
30	CCNT2	chr5:112111899-112112038	K562	blood:	n/a	n/a
31	CEBPB	chr5:112120449-112120736	IMR90	lung:	n/a	n/a
32	CEBPB	chr5:112112038-112112424	IMR90	lung:	n/a	n/a
33	CEBPB	chr5:112120462-112120708	HepG2	liver:	n/a	n/a
34	CEBPB	chr5:112066005-112066132	H1-hESC	embryonic stem cell:	n/a	chr5:112066085-112066098
35	CEBPB	chr5:112077233-112077496	K562	blood:	n/a	n/a
36	CEBPB	chr5:112115126-112115653	IMR90	lung:	n/a	chr5:112115337-112115348
37	CEBPB	chr5:112073149-112073774	Hela-S3	cervix:	n/a	chr5:112073516-112073524
38	CEBPB	chr5:112115159-112115510	A549	lung:	n/a	chr5:112115337-112115348
39	CEBPB	chr5:112065946-112066218	K562	blood:	n/a	chr5:112066085-112066098
40	CEBPB	chr5:112073461-112073640	A549	lung:	n/a	chr5:112073516-112073524
41	CEBPB	chr5:112122376-112122699	IMR90	lung:	n/a	n/a
42	CEBPB	chr5:112106567-112106720	IMR90	lung:	n/a	chr5:112106636-112106647
43	CEBPB	chr5:112104700-112104965	K562	blood:	n/a	n/a
44	CEBPB	chr5:112115167-112115502	HepG2	liver:	n/a	chr5:112115337-112115348
45	CEBPB	chr5:112122991-112123292	IMR90	lung:	n/a	n/a
46	CEBPB	chr5:112115171-112115504	K562	blood:	n/a	chr5:112115337-112115348
47	CEBPB	chr5:112120485-112120742	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr5:112115162-112115541	Hela-S3	cervix:	n/a	chr5:112115337-112115348
49	CEBPB	chr5:112057026-112057106	K562	blood:	n/a	n/a
50	CHD1	chr5:112073410-112073808	GM12878	blood:	n/a	chr5:112073658-112073668

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:112073769-112073819	HL-60	blood:	n/a
2	chr5:112073769-112073819	HL-60	blood:	n/a
3	chr5:112073426-112073476	HL-60	blood:	n/a
4	chr5:112074043-112074093	GM12892	blood:	n/a
5	chr5:112073350-112073400	H1-hESC	embryonic stem cell:	embryo
6	chr5:112073686-112073736	Jurkat	blood:	n/a
7	chr5:112073686-112073736	Hela-S3	cervix:	n/a
8	chr5:112073769-112073819	AG09309	skin:	n/a
9	chr5:112073769-112073819	BJ	skin:	n/a
10	chr5:112074043-112074093	AG04449	skin:	fetal
11	chr5:112073438-112073488	NH-A	brain:	n/a
12	chr5:112073373-112073423	HPAEpiC	pulmonary alveolar:	n/a
13	chr5:112073373-112073423	HL-60	blood:	n/a
14	chr5:112054378-112054428	Hepatocyte	liver:	n/a
15	chr5:112054378-112054428	RPTEC	kidney:	n/a
16	chr5:112073398-112073448	IMR90	lung:	fetal
17	chr5:112073398-112073448	HL-60	blood:	n/a
18	chr5:112073406-112073456	SKMC	muscle:	n/a
19	chr5:112073350-112073400	ECC-1	luminal epithelium:	n/a
20	chr5:112073544-112073594	PANC-1	pancreas:	n/a
21	chr5:112073502-112073552	HRPEpiC	eye:	n/a
22	chr5:112073769-112073819	SAEC	small airway:	n/a
23	chr5:112073769-112073819	A549	lung:	n/a
24	chr5:112073426-112073476	AG04449	skin:	fetal
25	chr5:112073686-112073736	HUVEC	blood vessel:	n/a
26	chr5:112073373-112073423	CMK	blood:	n/a
27	chr5:112054378-112054428	GM12891	blood:	n/a
28	chr5:112073348-112073398	HUVEC	blood vessel:	n/a
29	chr5:112073348-112073398	HMEC	breast:	n/a
30	chr5:112073348-112073398	NB4	blood:	n/a
31	chr5:112073426-112073476	BE2_C	brain:	n/a
32	chr5:112073433-112073483	AG04450	lung:	fetal
33	chr5:112073438-112073488	NB4	blood:	n/a
34	chr5:112073406-112073456	BJ	skin:	n/a
35	chr5:112073398-112073448	CMK	blood:	n/a
36	chr5:112074043-112074093	ECC-1	luminal epithelium:	n/a
37	chr5:112073348-112073398	HL-60	blood:	n/a
38	chr5:112073398-112073448	SK-N-SH	brain:	n/a
39	chr5:112073502-112073552	GM06990	blood:	n/a
40	chr5:112073433-112073483	HIPEpiC	eye:	n/a
41	chr5:112073348-112073398	BJ	skin:	n/a
42	chr5:112073373-112073423	Hepatocyte	liver:	n/a
43	chr5:112073373-112073423	T-47D	breast:	n/a
44	chr5:112073433-112073483	HCPEpiC	choroid plexus:	n/a
45	chr5:112073438-112073488	AG09309	skin:	n/a
46	chr5:112073406-112073456	HRCEpiC	kidney:	n/a
47	chr5:112073570-112073620	AG09319	gingival:	n/a
48	chr5:112054378-112054428	AoSMC	blood vessel:	n/a
49	chr5:112073438-112073488	HIPEpiC	eye:	n/a
50	chr5:112073538-112073588	CMK	blood:	n/a

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:112040661..112045747-chr5:112046493..112054139,9	MCF-7	breast:
2	chr5:112077462..112079150-chr5:112174470..112176548,2	K562	blood:
3	chr5:112070264..112074990-chr5:112075213..112080518,8	K562	blood:
4	chr5:112123801..112127041-chr5:112128309..112132302,4	K562	blood:
5	chr5:112065589..112068321-chr5:112080133..112082832,2	MCF-7	breast:
6	chr5:112036075..112039383-chr5:112077944..112080401,3	K562	blood:
7	chr5:112041510..112043623-chr5:112066965..112069551,3	MCF-7	breast:
8	chr5:112042859..112045192-chr5:112064227..112066122,2	K562	blood:
9	chr5:111496496..111498009-chr5:112089679..112091650,2	K562	blood:
10	chr5:112053239..112054814-chr5:112058793..112060310,2	K562	blood:
11	chr5:112121618..112123708-chr5:112137434..112139348,2	K562	blood:
12	chr5:112071994..112074935-chr5:112084057..112088000,3	K562	blood:
13	chr5:112058449..112061248-chr5:112063741..112066202,3	K562	blood:
14	chr5:112048029..112050157-chr5:112062177..112064729,3	K562	blood:
15	chr5:112053239..112054814-chr5:112058793..112060310,2	K562	blood:
16	chr5:112063462..112066944-chr5:112067899..112070429,3	K562	blood:
17	chr5:112048029..112050157-chr5:112062622..112064729,2	K562	blood:
18	chr5:112050398..112055694-chr5:112065977..112068837,5	K562	blood:
19	chr5:112026203..112028934-chr5:112090617..112094558,3	K562	blood:
20	chr5:112053751..112055842-chr5:112072998..112075540,2	K562	blood:
21	chr5:112065589..112068321-chr5:112080133..112082832,2	MCF-7	breast:
22	chr5:112026956..112028743-chr5:112092684..112094360,6	MCF-7	breast:
23	chr5:111496324..111497979-chr5:112068139..112070715,2	K562	blood:
24	chr5:111881988..111883507-chr5:112090046..112093045,2	MCF-7	breast:
25	chr5:112042397..112044645-chr5:112071738..112074273,3	MCF-7	breast:
26	chr5:112038553..112041521-chr5:112056606..112058817,2	K562	blood:
27	chr5:112056712..112059185-chr5:112067106..112069826,2	K562	blood:
28	chr5:112053504..112055952-chr5:112056185..112057959,2	MCF-7	breast:
29	chr5:112041486..112046402-chr5:112068342..112076365,12	K562	blood:
30	chr5:112043098..112044806-chr5:112058262..112061694,3	MCF-7	breast:
31	chr5:112089718..112092112-chr5:112180535..112183405,2	K562	blood:
32	chr5:112063462..112066944-chr5:112067899..112070429,3	K562	blood:
33	chr5:112064978..112067085-chr5:112072566..112074120,2	K562	blood:
34	chr5:112123613..112127041-chr5:112129146..112132302,3	K562	blood:
35	chr5:112058057..112061004-chr5:112174922..112177064,2	K562	blood:
36	chr5:112041940..112044616-chr5:112073343..112075090,3	MCF-7	breast:
37	chr5:112030715..112032884-chr5:112068786..112071232,2	K562	blood:
38	chr5:112026916..112029331-chr5:112092996..112093925,9	K562	blood:
39	chr5:112103979..112106564-chr5:112195241..112197726,2	K562	blood:
40	chr5:112060614..112062954-chr5:112069496..112072415,2	K562	blood:
41	chr5:112041705..112044841-chr5:112058087..112059989,3	K562	blood:
42	chr5:112121866..112123891-chr5:112136309..112139852,3	K562	blood:
43	chr5:112070188..112073138-chr5:112174884..112177444,2	K562	blood:
44	chr5:112040021..112044841-chr5:112056606..112060085,6	K562	blood:
45	chr5:112042040..112044749-chr5:112077105..112080754,4	K562	blood:
46	chr5:112018949..112022294-chr5:112089786..112092475,3	MCF-7	breast:
47	chr5:112050398..112055694-chr5:112065977..112068837,5	K562	blood:
48	chr5:112070801..112074184-chr5:112077517..112081527,4	K562	blood:
49	chr5:112097863..112099385-chr5:112105833..112108038,2	K562	blood:
50	chr5:112066564..112068742-chr5:112071367..112073488,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6-482P	TF binding region
APC	TF binding region
CBX3P3	TF binding region
RNU6-482P	CpG island
APC	CpG island
CBX3P3	CpG island
ENSG00000153037	chromatin interactions
ENSG00000251014	chromatin interactions
ENSG00000224032	chromatin interactions
ENSG00000238363	chromatin interactions
ENSG00000272869	chromatin interactions
ENSG00000134982	chromatin interactions

Extended variants
information (count: 3328 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:3328 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17134873	chr5:112053911-112053912	Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113036052	chr5:112053959-112053960	Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs144085706	chr5:112053961-112053962	Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs573809234	chr5:112053996-112053997	Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs536675698	chr5:112054082-112054083	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs6864688	chr5:112054086-112054087	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs575509464	chr5:112054094-112054095	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs556290466	chr5:112054150-112054151	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs577525491	chr5:112054158-112054159	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs560151393	chr5:112054175-112054176	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544857655	chr5:112054179-112054180	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs557769831	chr5:112054191-112054192	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs572885757	chr5:112054202-112054203	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs115648598	chr5:112054204-112054205	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs562062227	chr5:112054243-112054244	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs200004079	chr5:112054256-112054257	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs542784081	chr5:112054266-112054267	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs184954640	chr5:112054270-112054271	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs544486475	chr5:112054307-112054308	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs2464812	chr5:112054322-112054323	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs146044281	chr5:112054352-112054353	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs574345148	chr5:112054441-112054442	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs557630495	chr5:112054445-112054446	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs74890534	chr5:112054457-112054458	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs9326862	chr5:112054547-112054548	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs548936643	chr5:112054571-112054572	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs139966529	chr5:112054595-112054596	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs537906955	chr5:112054697-112054698	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs144206564	chr5:112054713-112054714	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs571100994	chr5:112054807-112054808	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs538581274	chr5:112054817-112054818	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs553626743	chr5:112054842-112054843	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs571980156	chr5:112054895-112054896	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs540282272	chr5:112054906-112054907	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs533288748	chr5:112054910-112054911	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs7726765	chr5:112054913-112054914	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs371757938	chr5:112054917-112054918	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs190986573	chr5:112054934-112054935	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs1616230	chr5:112055008-112055009	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs563117602	chr5:112055058-112055059	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs142310350	chr5:112055071-112055072	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs79644413	chr5:112055082-112055083	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs545746379	chr5:112055110-112055111	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs549761329	chr5:112055164-112055165	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs151270252	chr5:112055174-112055175	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs550443158	chr5:112055238-112055239	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs548713778	chr5:112055260-112055261	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs567206975	chr5:112055276-112055277	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs369594631	chr5:112055282-112055283	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs113774877	chr5:112055306-112055307	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	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
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Colorectal cancer	21297112	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	21518781	CNVD
Prostate cancer	22341455	CNVD
Lung cancer	20668451	CNVD
adenomatous polyposis	20649969	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Colorectal cancer	22014273	CNVD
Colorectal cancer	23471846	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2003 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:112044800-112058000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr5:112044800-112058800	Weak transcription	Fetal Muscle Trunk	muscle
3	chr5:112045200-112054000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr5:112045400-112054400	Weak transcription	NHEK	skin
5	chr5:112045400-112062000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr5:112045600-112054000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr5:112045600-112054600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:112045600-112060200	Weak transcription	NHLF	lung
9	chr5:112045600-112061600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr5:112045600-112063600	Weak transcription	Ovary	ovary
11	chr5:112045800-112054000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr5:112046000-112054000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr5:112046000-112069200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr5:112047000-112060400	Weak transcription	Primary B cells from peripheral blood	blood
15	chr5:112047000-112061600	Weak transcription	Aorta	Aorta
16	chr5:112047000-112066000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr5:112047200-112054000	Weak transcription	Right Ventricle	heart
18	chr5:112047400-112054000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr5:112047400-112056200	Weak transcription	Dnd41	blood
20	chr5:112047400-112058600	Weak transcription	Stomach Smooth Muscle	stomach
21	chr5:112047400-112060400	Weak transcription	Fetal Intestine Large	intestine
22	chr5:112047400-112072400	Weak transcription	Thymus	Thymus
23	chr5:112047600-112054000	Weak transcription	Pancreas	Pancrea
24	chr5:112047600-112061600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr5:112048200-112054000	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr5:112048200-112054000	Weak transcription	Gastric	stomach
27	chr5:112048200-112058200	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr5:112048400-112061200	Weak transcription	Fetal Intestine Small	intestine
29	chr5:112049200-112054000	Weak transcription	Brain Angular Gyrus	brain
30	chr5:112049200-112054000	Weak transcription	Brain Cingulate Gyrus	brain
31	chr5:112049200-112054000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr5:112049200-112054200	Weak transcription	Colon Smooth Muscle	Colon
33	chr5:112049200-112061600	Weak transcription	Fetal Stomach	stomach
34	chr5:112049600-112054000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr5:112049600-112054000	Weak transcription	Left Ventricle	heart
36	chr5:112049600-112054000	Weak transcription	Psoas Muscle	Psoas
37	chr5:112049600-112054000	Weak transcription	Small Intestine	intestine
38	chr5:112049600-112054200	Weak transcription	Brain Hippocampus Middle	brain
39	chr5:112049600-112055800	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr5:112049600-112060400	Weak transcription	Lung	lung
41	chr5:112050200-112054000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr5:112050200-112056200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr5:112050600-112054200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr5:112050800-112054200	Weak transcription	Brain Anterior Caudate	brain
45	chr5:112050800-112056200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr5:112051000-112056200	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr5:112051200-112058600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr5:112051400-112054000	Weak transcription	Brain Substantia Nigra	brain
49	chr5:112052000-112072600	Weak transcription	Primary B cells from cord blood	blood
50	chr5:112052600-112054000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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