Variant report

Variant	nsv1032155
Chromosome Location	chr8:124609702-124739559
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1698)
CpG islands
(count:1405)
Chromatin interactive
region (count:192)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1698 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:124731904-124732876	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:124733113-124733385	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:124618722-124618755	K562	blood:	n/a	n/a
4	ARID3A	chr8:124720190-124720444	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:124642285-124643008	K562	blood:	n/a	n/a
6	ARID3A	chr8:124643255-124643748	K562	blood:	n/a	n/a
7	ARID3A	chr8:124631699-124632320	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:124665906-124666122	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:124670470-124670670	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:124625694-124625864	K562	blood:	n/a	n/a
11	ARID3A	chr8:124681724-124681853	K562	blood:	n/a	n/a
12	ATF1	chr8:124643377-124643724	K562	blood:	n/a	n/a
13	ATF1	chr8:124656452-124656561	K562	blood:	n/a	n/a
14	ATF1	chr8:124681592-124681838	K562	blood:	n/a	n/a
15	ATF1	chr8:124625567-124625811	K562	blood:	n/a	n/a
16	ATF1	chr8:124642614-124642958	K562	blood:	n/a	n/a
17	ATF1	chr8:124634920-124635284	K562	blood:	n/a	n/a
18	ATF2	chr8:124683273-124683671	GM12878	blood:	n/a	n/a
19	ATF3	chr8:124642531-124642920	K562	blood:	n/a	n/a
20	ATF3	chr8:124729935-124730196	K562	blood:	n/a	n/a
21	ATF3	chr8:124618542-124618964	K562	blood:	n/a	n/a
22	ATF3	chr8:124643405-124643738	K562	blood:	n/a	n/a
23	BACH1	chr8:124642426-124643091	K562	blood:	n/a	n/a
24	BACH1	chr8:124615227-124615311	K562	blood:	n/a	n/a
25	BATF	chr8:124734902-124735085	GM12878	blood:	n/a	n/a
26	BATF	chr8:124683307-124683622	GM12878	blood:	n/a	n/a
27	BATF	chr8:124625606-124625885	GM12878	blood:	n/a	chr8:124625763-124625774
28	BATF	chr8:124683266-124683730	GM12878	blood:	n/a	n/a
29	BCL11A	chr8:124683294-124683693	GM12878	blood:	n/a	chr8:124683395-124683404 chr8:124683396-124683405
30	BCL3	chr8:124658092-124658418	GM12878	blood:	n/a	n/a
31	BCL3	chr8:124690167-124690528	GM12878	blood:	n/a	n/a
32	BHLHE40	chr8:124681712-124681806	K562	blood:	n/a	n/a
33	BHLHE40	chr8:124643433-124643641	K562	blood:	n/a	n/a
34	BHLHE40	chr8:124729908-124730268	K562	blood:	n/a	n/a
35	BHLHE40	chr8:124706038-124706279	K562	blood:	n/a	n/a
36	BHLHE40	chr8:124628995-124629314	K562	blood:	n/a	n/a
37	BHLHE40	chr8:124732035-124732650	HepG2	liver:	n/a	n/a
38	BHLHE40	chr8:124642548-124643227	K562	blood:	n/a	n/a
39	BHLHE40	chr8:124706099-124706391	A549	lung:	n/a	n/a
40	BHLHE40	chr8:124635034-124635336	K562	blood:	n/a	n/a
41	BHLHE40	chr8:124647465-124647763	K562	blood:	n/a	n/a
42	BHLHE40	chr8:124631890-124632269	HepG2	liver:	n/a	n/a
43	BHLHE40	chr8:124666560-124666714	K562	blood:	n/a	n/a
44	CBX3	chr8:124642535-124642938	K562	blood:	n/a	n/a
45	CBX3	chr8:124702447-124702987	HCT-116	colon:	n/a	n/a
46	CBX3	chr8:124631424-124631796	K562	blood:	n/a	n/a
47	CBX3	chr8:124679708-124680048	K562	blood:	n/a	n/a
48	CBX3	chr8:124683048-124684029	HCT-116	colon:	n/a	n/a
49	CBX3	chr8:124631445-124631755	K562	blood:	n/a	n/a
50	CBX3	chr8:124729852-124730263	K562	blood:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:124730169-124730219	MCF10A-Er-Src	breast:	n/a
2	chr8:124632130-124632180	MCF10A-Er-Src	breast:	n/a
3	chr8:124730169-124730219	MCF10A-Er-Src	breast:	n/a
4	chr8:124632130-124632180	MCF10A-Er-Src	breast:	n/a
5	chr8:124644256-124644306	PFSK-1	brain:	n/a
6	chr8:124665293-124665343	AG04450	lung:	fetal
7	chr8:124666123-124666173	HepG2	liver:	n/a
8	chr8:124666123-124666173	HRE	kidney:	n/a
9	chr8:124704218-124704268	AG10803	skin:	n/a
10	chr8:124730225-124730275	MCF10A-Er-Src	breast:	n/a
11	chr8:124730169-124730219	HCPEpiC	choroid plexus:	n/a
12	chr8:124700752-124700802	HAEpiC	amniotic membrane:	n/a
13	chr8:124704218-124704268	Jurkat	blood:	n/a
14	chr8:124658075-124658125	Caco-2	colon:	n/a
15	chr8:124665016-124665066	NT2-D1	testis:	n/a
16	chr8:124693755-124693805	K562	blood:	n/a
17	chr8:124658075-124658125	HCT-116	colon:	n/a
18	chr8:124688770-124688820	PFSK-1	brain:	n/a
19	chr8:124665838-124665888	MCF10A-Er-Src	breast:	n/a
20	chr8:124693396-124693446	Jurkat	blood:	n/a
21	chr8:124693396-124693446	HMEC	breast:	n/a
22	chr8:124658075-124658125	Jurkat	blood:	n/a
23	chr8:124720897-124720947	PFSK-1	brain:	n/a
24	chr8:124730091-124730141	SK-N-MC	brain:	n/a
25	chr8:124688770-124688820	SK-N-SH	brain:	n/a
26	chr8:124700752-124700802	SK-N-MC	brain:	n/a
27	chr8:124693755-124693805	Hela-S3	cervix:	n/a
28	chr8:124658075-124658125	GM12891	blood:	n/a
29	chr8:124665021-124665071	HCT-116	colon:	n/a
30	chr8:124658143-124658193	HIPEpiC	eye:	n/a
31	chr8:124730225-124730275	SKMC	muscle:	n/a
32	chr8:124665021-124665071	A549	lung:	n/a
33	chr8:124665021-124665071	HCF	heart:	n/a
34	chr8:124665021-124665071	H1-hESC	embryonic stem cell:	embryo
35	chr8:124693396-124693446	ovcar-3	ovarian:	n/a
36	chr8:124732088-124732138	ECC-1	luminal epithelium:	n/a
37	chr8:124658104-124658154	HCM	heart:	n/a
38	chr8:124665016-124665066	LNCaP	prostate:	n/a
39	chr8:124693396-124693446	BJ	skin:	n/a
40	chr8:124693755-124693805	PFSK-1	brain:	n/a
41	chr8:124665838-124665888	BE2_C	brain:	n/a
42	chr8:124720897-124720947	AG04449	skin:	fetal
43	chr8:124730169-124730219	PFSK-1	brain:	n/a
44	chr8:124665016-124665066	Hela-S3	cervix:	n/a
45	chr8:124688770-124688820	BE2_C	brain:	n/a
46	chr8:124658075-124658125	SK-N-MC	brain:	n/a
47	chr8:124657935-124657985	HRCEpiC	kidney:	n/a
48	chr8:124700752-124700802	HCM	heart:	n/a
49	chr8:124665293-124665343	HL-60	blood:	n/a
50	chr8:124657935-124657985	NT2-D1	testis:	n/a

(count:192 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr8:124474931..124475567-chr8:124708452..124709447,2	MCF-7	breast:
2	chr8:124656144..124657737-chr8:124658420..124660682,2	MCF-7	breast:
3	chr8:124705717..124707673-chr8:124709259..124711707,2	K562	blood:
4	chr8:124481286..124483387-chr8:124686778..124689614,2	K562	blood:
5	chr8:124717663..124720298-chr8:124732166..124733821,2	MCF-7	breast:
6	chr8:124651607..124653869-chr8:124656583..124659283,2	MCF-7	breast:
7	chr8:124637710..124639929-chr8:124649061..124650704,2	K562	blood:
8	chr8:124662032..124665488-chr8:124668654..124670370,3	MCF-7	breast:
9	chr8:124606691..124608207-chr8:124623300..124624802,2	MCF-7	breast:
10	chr8:124653035..124654923-chr8:124661285..124663313,2	MCF-7	breast:
11	chr8:124721349..124725148-chr8:124726476..124729073,3	MCF-7	breast:
12	chr8:124635851..124638436-chr8:124639907..124645326,4	MCF-7	breast:
13	chr8:124637710..124639929-chr8:124649061..124650704,2	K562	blood:
14	chr8:124721349..124725148-chr8:124726476..124729073,3	MCF-7	breast:
15	chr8:124637761..124639286-chr8:124642361..124644440,2	MCF-7	breast:
16	chr8:124597117..124599176-chr8:124606571..124610166,3	MCF-7	breast:
17	chr8:124704299..124706961-chr8:124708389..124710569,2	MCF-7	breast:
18	chr8:124655670..124657756-chr8:124660016..124662293,2	K562	blood:
19	chr8:124498774..124501507-chr8:124732640..124734815,2	MCF-7	breast:
20	chr8:124643258..124644911-chr8:124705316..124706852,2	MCF-7	breast:
21	chr8:124699483..124702834-chr8:124703972..124707489,4	MCF-7	breast:
22	chr8:124619293..124622384-chr8:124622665..124625911,4	MCF-7	breast:
23	chr8:124631690..124636350-chr8:124636820..124639230,5	MCF-7	breast:
24	chr8:124731732..124734345-chr8:124745341..124747326,2	MCF-7	breast:
25	chr8:124618052..124619899-chr8:124628853..124631405,2	MCF-7	breast:
26	chr8:124645881..124648835-chr8:124656930..124658613,2	K562	blood:
27	chr8:124692787..124694393-chr8:124696495..124698198,2	MCF-7	breast:
28	chr8:124658511..124660585-chr8:124661818..124664986,4	MCF-7	breast:
29	chr8:124651070..124655154-chr8:124655316..124659808,4	MCF-7	breast:
30	chr8:124718415..124720080-chr8:124724690..124726848,2	MCF-7	breast:
31	chr8:124643571..124646557-chr8:124651939..124654675,2	MCF-7	breast:
32	chr8:124474442..124476967-chr8:124689689..124692610,2	MCF-7	breast:
33	chr8:124551901..124554787-chr8:124705917..124707799,2	MCF-7	breast:
34	chr8:124630464..124632605-chr8:124778589..124780623,2	MCF-7	breast:
35	chr8:124474750..124475700-chr8:124705653..124706300,2	MCF-7	breast:
36	chr8:124578047..124580676-chr8:124642644..124645333,2	MCF-7	breast:
37	chr8:124651070..124655154-chr8:124655316..124659808,4	MCF-7	breast:
38	chr8:124551934..124554097-chr8:124626463..124629241,3	MCF-7	breast:
39	chr8:124642600..124645867-chr8:124673711..124676775,3	MCF-7	breast:
40	chr8:124614662..124616733-chr8:124630973..124633484,2	MCF-7	breast:
41	chr8:124694373..124696517-chr8:124701551..124703727,2	K562	blood:
42	chr8:124714538..124716840-chr8:124716976..124719629,2	MCF-7	breast:
43	chr8:124705081..124707705-chr8:124777857..124780105,2	MCF-7	breast:
44	chr8:124668534..124670111-chr8:124695984..124698883,2	K562	blood:
45	chr8:124673351..124678204-chr8:124678247..124683296,7	MCF-7	breast:
46	chr8:124576323..124577993-chr8:124681885..124683478,2	MCF-7	breast:
47	chr8:124608092..124610186-chr8:124645249..124647691,2	MCF-7	breast:
48	chr8:124668666..124670546-chr8:124672499..124675168,2	MCF-7	breast:
49	chr8:124621417..124623503-chr8:124631883..124634146,2	MCF-7	breast:
50	chr8:124694373..124696517-chr8:124701551..124703727,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM91A1-1	chr8:124637927-124638001	ENSG00000253286.1
2	lnc-FAM91A1-1	chr8:124628966-124629083	NONHSAT128562
3	lnc-FAM91A1-1	chr8:124626465-124626515	ENSG00000253286.1
4	lnc-KLHL38-1	chr8:124723873-124724993	NONHSAT128564
5	lnc-FAM91A1-1	chr8:124628966-124629083	ENSG00000253286.1
6	lnc-FAM91A1-1	chr8:124651742-124651884	ENSG00000253286.1
7	lnc-FAM91A1-1	chr8:124628966-124629083	ENSG00000253286.1
8	lnc-FAM91A1-1	chr8:124626465-124626515	ENSG00000253286.1
9	lnc-FAM91A1-1	chr8:124626465-124627051	NONHSAT128562
10	lnc-FAM91A1-1	chr8:124646554-124646660	ENSG00000253286.1
11	lnc-FAM91A1-1	chr8:124651134-124651257	ENSG00000253286.1
12	lnc-FAM91A1-1	chr8:124670489-124670810	ENSG00000253286.1

No data

Variant related genes	Relation type
KLHL38	TF binding region
ENSG00000253286	TF binding region
KLHL38	CpG island
ENSG00000253286	CpG island
ENSG00000175946	chromatin interactions
ENSG00000104537	chromatin interactions
ENSG00000176853	chromatin interactions
ENSG00000156804	chromatin interactions
ENSG00000253286	chromatin interactions
ENSG00000251840	chromatin interactions

Extended variants
information (count: 5430 )
Associated
traits (count: 153 )

Variant overlapped rSNPs/rCNVs (count:5430 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372361147	chr8:124609711-124609712	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs377157017	chr8:124609721-124609722	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs140360995	chr8:124609784-124609785	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs144218824	chr8:124609798-124609799	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs55987314	chr8:124609801-124609802	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs536892131	chr8:124609804-124609805	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs537351443	chr8:124609832-124609833	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs557018873	chr8:124609843-124609844	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs73335873	chr8:124609850-124609851	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs539280737	chr8:124609877-124609878	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs552624347	chr8:124609916-124609917	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs116442000	chr8:124609928-124609929	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs182992058	chr8:124609940-124609941	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371325295	chr8:124609976-124609977	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs575197777	chr8:124609994-124609995	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs62520908	chr8:124610021-124610022	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs564661712	chr8:124610080-124610081	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs2385450	chr8:124610112-124610113	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs2385449	chr8:124610131-124610132	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs186951446	chr8:124610165-124610166	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs58847541	chr8:124610166-124610167	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs111260481	chr8:124610182-124610183	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs13273000	chr8:124610213-124610214	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs59488911	chr8:124610228-124610229	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs191852964	chr8:124610260-124610261	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs550833990	chr8:124610269-124610270	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs570680816	chr8:124610394-124610395	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs28490413	chr8:124610430-124610431	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs546400610	chr8:124610457-124610458	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs566185986	chr8:124610458-124610459	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs535176459	chr8:124610506-124610507	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs555213045	chr8:124610507-124610508	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs6470158	chr8:124610521-124610522	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs6470159	chr8:124610526-124610527	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs6470160	chr8:124610561-124610562	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs372762258	chr8:124610579-124610580	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs187883484	chr8:124610650-124610651	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs540787864	chr8:124610653-124610654	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs560670357	chr8:124610654-124610655	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs574327768	chr8:124610658-124610659	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs193017588	chr8:124610681-124610682	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs528536338	chr8:124610688-124610689	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs562873635	chr8:124610720-124610721	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs531707570	chr8:124610759-124610760	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs7830837	chr8:124610841-124610842	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs551501019	chr8:124610846-124610847	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs564367302	chr8:124610910-124610911	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs28825116	chr8:124611004-124611005	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs546539506	chr8:124611005-124611006	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs111367289	chr8:124611025-124611026	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:153)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	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
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	17375183	CNVD

Chromatin state (count:2251 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124605000-124609800	Weak transcription	Colon Smooth Muscle	Colon
2	chr8:124608000-124610400	Enhancers	Esophagus	oesophagus
3	chr8:124608600-124609800	Enhancers	Psoas Muscle	Psoas
4	chr8:124608600-124610200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:124608600-124610400	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr8:124608600-124610400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr8:124608600-124610400	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr8:124608600-124610400	Enhancers	HMEC	breast
9	chr8:124608600-124610400	Enhancers	HSMMtube	muscle
10	chr8:124608800-124609800	Enhancers	Placenta	Placenta
11	chr8:124608800-124610200	Enhancers	Osteobl	bone
12	chr8:124609000-124610400	Enhancers	HSMM	muscle
13	chr8:124609200-124609800	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr8:124609200-124610200	Weak transcription	Stomach Smooth Muscle	stomach
15	chr8:124609200-124610400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr8:124609200-124610400	Enhancers	Aorta	Aorta
17	chr8:124609200-124610400	Enhancers	Pancreas	Pancrea
18	chr8:124609200-124610400	Enhancers	Right Atrium	heart
19	chr8:124609200-124615000	Weak transcription	Fetal Intestine Small	intestine
20	chr8:124609400-124610200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr8:124609600-124609800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr8:124609600-124610200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr8:124609600-124610400	Enhancers	Rectal Smooth Muscle	rectum
24	chr8:124609800-124610000	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr8:124609800-124610200	Enhancers	Colon Smooth Muscle	Colon
26	chr8:124609800-124620800	Weak transcription	Psoas Muscle	Psoas
27	chr8:124610200-124610400	Enhancers	Stomach Smooth Muscle	stomach
28	chr8:124610400-124611400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr8:124610400-124618600	Weak transcription	HMEC	breast
30	chr8:124610400-124620200	Weak transcription	Pancreas	Pancrea
31	chr8:124610400-124628000	Weak transcription	Aorta	Aorta
32	chr8:124610400-124630000	Weak transcription	Right Atrium	heart
33	chr8:124611400-124615200	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr8:124614400-124615200	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr8:124615000-124615400	Enhancers	Fetal Intestine Small	intestine
36	chr8:124615000-124615600	Enhancers	K562	blood
37	chr8:124615200-124617200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr8:124615400-124617400	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr8:124615600-124618000	Weak transcription	K562	blood
40	chr8:124616000-124617200	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr8:124617200-124620000	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr8:124618000-124619400	Enhancers	K562	blood
43	chr8:124618200-124619200	Enhancers	Ovary	ovary
44	chr8:124618600-124619200	Enhancers	HMEC	breast
45	chr8:124618800-124619200	Enhancers	NH-A	brain
46	chr8:124618800-124619600	Enhancers	Fetal Intestine Large	intestine
47	chr8:124618800-124619600	Enhancers	Fetal Intestine Small	intestine
48	chr8:124619000-124619600	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr8:124619000-124619600	Enhancers	Small Intestine	intestine
50	chr8:124619200-124629800	Weak transcription	Ovary	ovary

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