Variant report

Variant	nsv612140
Chromosome Location	chr8:124604759-124738618
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1786)
CpG islands
(count:1405)
Chromatin interactive
region (count:202)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1786 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:124618722-124618755	K562	blood:	n/a	n/a
2	ARID3A	chr8:124665906-124666122	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:124670470-124670670	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:124733113-124733385	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:124642285-124643008	K562	blood:	n/a	n/a
6	ARID3A	chr8:124731904-124732876	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:124681724-124681853	K562	blood:	n/a	n/a
8	ARID3A	chr8:124625694-124625864	K562	blood:	n/a	n/a
9	ARID3A	chr8:124631699-124632320	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:124643255-124643748	K562	blood:	n/a	n/a
11	ARID3A	chr8:124720190-124720444	HepG2	liver:	n/a	n/a
12	ATF1	chr8:124625567-124625811	K562	blood:	n/a	n/a
13	ATF1	chr8:124681592-124681838	K562	blood:	n/a	n/a
14	ATF1	chr8:124643377-124643724	K562	blood:	n/a	n/a
15	ATF1	chr8:124634920-124635284	K562	blood:	n/a	n/a
16	ATF1	chr8:124642614-124642958	K562	blood:	n/a	n/a
17	ATF1	chr8:124604689-124605011	K562	blood:	n/a	n/a
18	ATF1	chr8:124656452-124656561	K562	blood:	n/a	n/a
19	ATF2	chr8:124683273-124683671	GM12878	blood:	n/a	n/a
20	ATF3	chr8:124642531-124642920	K562	blood:	n/a	n/a
21	ATF3	chr8:124729935-124730196	K562	blood:	n/a	n/a
22	ATF3	chr8:124618542-124618964	K562	blood:	n/a	n/a
23	ATF3	chr8:124604758-124604927	K562	blood:	n/a	n/a
24	ATF3	chr8:124604712-124604954	K562	blood:	n/a	n/a
25	ATF3	chr8:124643405-124643738	K562	blood:	n/a	n/a
26	BACH1	chr8:124615227-124615311	K562	blood:	n/a	n/a
27	BACH1	chr8:124642426-124643091	K562	blood:	n/a	n/a
28	BATF	chr8:124625606-124625885	GM12878	blood:	n/a	chr8:124625763-124625774
29	BATF	chr8:124683266-124683730	GM12878	blood:	n/a	n/a
30	BATF	chr8:124734902-124735085	GM12878	blood:	n/a	n/a
31	BATF	chr8:124683307-124683622	GM12878	blood:	n/a	n/a
32	BCL11A	chr8:124683294-124683693	GM12878	blood:	n/a	chr8:124683395-124683404 chr8:124683396-124683405
33	BCL3	chr8:124690167-124690528	GM12878	blood:	n/a	n/a
34	BCL3	chr8:124658092-124658418	GM12878	blood:	n/a	n/a
35	BHLHE40	chr8:124635034-124635336	K562	blood:	n/a	n/a
36	BHLHE40	chr8:124706038-124706279	K562	blood:	n/a	n/a
37	BHLHE40	chr8:124666560-124666714	K562	blood:	n/a	n/a
38	BHLHE40	chr8:124604729-124604963	K562	blood:	n/a	n/a
39	BHLHE40	chr8:124732035-124732650	HepG2	liver:	n/a	n/a
40	BHLHE40	chr8:124729908-124730268	K562	blood:	n/a	n/a
41	BHLHE40	chr8:124681712-124681806	K562	blood:	n/a	n/a
42	BHLHE40	chr8:124647465-124647763	K562	blood:	n/a	n/a
43	BHLHE40	chr8:124631890-124632269	HepG2	liver:	n/a	n/a
44	BHLHE40	chr8:124642548-124643227	K562	blood:	n/a	n/a
45	BHLHE40	chr8:124643433-124643641	K562	blood:	n/a	n/a
46	BHLHE40	chr8:124706099-124706391	A549	lung:	n/a	n/a
47	BHLHE40	chr8:124628995-124629314	K562	blood:	n/a	n/a
48	CBX3	chr8:124702491-124702872	K562	blood:	n/a	n/a
49	CBX3	chr8:124631424-124631796	K562	blood:	n/a	n/a
50	CBX3	chr8:124642535-124642938	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	chr8:124632130-124632180	HRCEpiC	kidney:	n/a
2	chr8:124658104-124658154	PrEC	prostate:	n/a
3	chr8:124632130-124632180	HRCEpiC	kidney:	n/a
4	chr8:124658104-124658154	PrEC	prostate:	n/a
5	chr8:124720897-124720947	NHDF-neo	bronchial:	n/a
6	chr8:124658143-124658193	ECC-1	luminal epithelium:	n/a
7	chr8:124700752-124700802	PFSK-1	brain:	n/a
8	chr8:124666123-124666173	HL-60	blood:	n/a
9	chr8:124658104-124658154	AG09319	gingival:	n/a
10	chr8:124730091-124730141	Hepatocyte	liver:	n/a
11	chr8:124720897-124720947	HepG2	liver:	n/a
12	chr8:124658075-124658125	GM12891	blood:	n/a
13	chr8:124657935-124657985	K562	blood:	n/a
14	chr8:124730225-124730275	HRE	kidney:	n/a
15	chr8:124632130-124632180	GM19239	blood:	n/a
16	chr8:124656433-124656483	HRE	kidney:	n/a
17	chr8:124665016-124665066	MCF-7	breast:	n/a
18	chr8:124625011-124625061	AG09319	gingival:	n/a
19	chr8:124700752-124700802	RPTEC	kidney:	n/a
20	chr8:124657935-124657985	LNCaP	prostate:	n/a
21	chr8:124658143-124658193	HEEpiC	esophagus:	n/a
22	chr8:124688770-124688820	GM12892	blood:	n/a
23	chr8:124625011-124625061	NH-A	brain:	n/a
24	chr8:124704218-124704268	Hela-S3	cervix:	n/a
25	chr8:124666123-124666173	HIPEpiC	eye:	n/a
26	chr8:124700752-124700802	MCF10A-Er-Src	breast:	n/a
27	chr8:124644256-124644306	MCF-7	breast:	n/a
28	chr8:124688770-124688820	HAEpiC	amniotic membrane:	n/a
29	chr8:124665021-124665071	GM12891	blood:	n/a
30	chr8:124720897-124720947	HNPCEpiC	eye:	n/a
31	chr8:124632130-124632180	LNCaP	prostate:	n/a
32	chr8:124665021-124665071	T-47D	breast:	n/a
33	chr8:124658143-124658193	NT2-D1	testis:	n/a
34	chr8:124700752-124700802	HNPCEpiC	eye:	n/a
35	chr8:124665021-124665071	GM12878	blood:	n/a
36	chr8:124625011-124625061	MCF-7	breast:	n/a
37	chr8:124730169-124730219	SK-N-SH	brain:	n/a
38	chr8:124665016-124665066	RPTEC	kidney:	n/a
39	chr8:124657935-124657985	HMEC	breast:	n/a
40	chr8:124658104-124658154	GM06990	blood:	n/a
41	chr8:124693755-124693805	AG04450	lung:	fetal
42	chr8:124666123-124666173	H1-hESC	embryonic stem cell:	embryo
43	chr8:124657935-124657985	HCPEpiC	choroid plexus:	n/a
44	chr8:124658143-124658193	AG09309	skin:	n/a
45	chr8:124665016-124665066	U87	brain:	n/a
46	chr8:124688770-124688820	SKMC	muscle:	n/a
47	chr8:124665838-124665888	BJ	skin:	n/a
48	chr8:124693755-124693805	HMEC	breast:	n/a
49	chr8:124693396-124693446	AG10803	skin:	n/a
50	chr8:124644256-124644306	PANC-1	pancreas:	n/a

(count:202 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr8:124696805..124699450-chr8:124701410..124703172,3	K562	blood:
2	chr8:124539471..124542410-chr8:124630471..124632625,2	MCF-7	breast:
3	chr8:124637761..124639286-chr8:124642361..124644440,2	MCF-7	breast:
4	chr8:124597117..124599176-chr8:124606571..124610166,3	MCF-7	breast:
5	chr8:124606691..124608207-chr8:124623300..124624802,2	MCF-7	breast:
6	chr8:124642600..124645867-chr8:124673711..124676775,3	MCF-7	breast:
7	chr8:124635355..124637919-chr8:124639810..124642059,2	MCF-7	breast:
8	chr8:124659242..124661407-chr8:124671915..124673705,2	MCF-7	breast:
9	chr8:124635851..124638436-chr8:124639907..124645326,4	MCF-7	breast:
10	chr8:124631690..124636350-chr8:124636820..124639230,5	MCF-7	breast:
11	chr8:124617135..124619248-chr8:124619400..124621074,2	K562	blood:
12	chr8:124724921..124730373-chr8:124736331..124739502,4	MCF-7	breast:
13	chr8:124730999..124733466-chr8:124735064..124737504,2	MCF-7	breast:
14	chr8:124694373..124696517-chr8:124701551..124703727,2	K562	blood:
15	chr8:124699483..124702834-chr8:124703972..124707489,4	MCF-7	breast:
16	chr8:124673351..124678204-chr8:124678247..124683296,7	MCF-7	breast:
17	chr8:124645881..124648835-chr8:124656930..124658613,2	K562	blood:
18	chr8:124668666..124670546-chr8:124672499..124675168,2	MCF-7	breast:
19	chr8:124575528..124576396-chr8:124638141..124638658,2	MCF-7	breast:
20	chr8:124581523..124583761-chr8:124647181..124648699,2	MCF-7	breast:
21	chr8:124498534..124499471-chr8:124705766..124706884,10	MCF-7	breast:
22	chr8:124481286..124483387-chr8:124686778..124689614,2	K562	blood:
23	chr8:124714538..124716840-chr8:124716976..124719629,2	MCF-7	breast:
24	chr8:124706375..124708121-chr8:124708408..124710117,2	MCF-7	breast:
25	chr8:124635851..124638436-chr8:124639907..124645326,4	MCF-7	breast:
26	chr8:124656144..124657737-chr8:124658420..124660682,2	MCF-7	breast:
27	chr8:124654411..124657402-chr8:124657666..124660616,2	K562	blood:
28	chr8:124618052..124619899-chr8:124628853..124631405,2	MCF-7	breast:
29	chr8:124658511..124660585-chr8:124661818..124664986,4	MCF-7	breast:
30	chr8:124647506..124650348-chr8:124660565..124662892,2	MCF-7	breast:
31	chr8:124630537..124633840-chr8:124641197..124643373,3	MCF-7	breast:
32	chr8:124624778..124629364-chr8:124635869..124639568,5	MCF-7	breast:
33	chr8:124606659..124608342-chr8:124651768..124654525,2	MCF-7	breast:
34	chr8:124692787..124694393-chr8:124696495..124698198,2	MCF-7	breast:
35	chr8:124662032..124665488-chr8:124668654..124670370,3	MCF-7	breast:
36	chr8:124721349..124725148-chr8:124726476..124729073,3	MCF-7	breast:
37	chr8:124705717..124707673-chr8:124709259..124711707,2	K562	blood:
38	chr8:124607569..124610027-chr8:124612022..124613929,3	MCF-7	breast:
39	chr8:124674081..124675971-chr8:124683411..124685005,2	MCF-7	breast:
40	chr8:124717663..124720298-chr8:124732166..124733821,2	MCF-7	breast:
41	chr8:124688958..124691412-chr8:124692898..124695103,2	K562	blood:
42	chr8:124630537..124633840-chr8:124641197..124643373,3	MCF-7	breast:
43	chr8:124637761..124639286-chr8:124642361..124644440,2	MCF-7	breast:
44	chr8:124559237..124561974-chr8:124607116..124608954,2	MCF-7	breast:
45	chr8:124662099..124664193-chr8:124664462..124666029,2	MCF-7	breast:
46	chr8:124647506..124650348-chr8:124660565..124662892,2	MCF-7	breast:
47	chr8:124608823..124611776-chr8:124612994..124616282,3	MCF-7	breast:
48	chr8:124475204..124475707-chr8:124705564..124706170,2	K562	blood:
49	chr8:124551934..124554097-chr8:124626463..124629241,3	MCF-7	breast:
50	chr8:124644904..124649137-chr8:124652807..124658443,6	MCF-7	breast:

(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	chr8:124626465-124627051	NONHSAT128562
3	lnc-FAM91A1-1	chr8:124670489-124670810	ENSG00000253286.1
4	lnc-FAM91A1-1	chr8:124626465-124626515	ENSG00000253286.1
5	lnc-FAM91A1-1	chr8:124628966-124629083	ENSG00000253286.1
6	lnc-FAM91A1-1	chr8:124651134-124651257	ENSG00000253286.1
7	lnc-FAM91A1-1	chr8:124651742-124651884	ENSG00000253286.1
8	lnc-FAM91A1-1	chr8:124626465-124626515	ENSG00000253286.1
9	lnc-FAM91A1-1	chr8:124628966-124629083	ENSG00000253286.1
10	lnc-KLHL38-1	chr8:124723873-124724993	NONHSAT128564
11	lnc-FAM91A1-1	chr8:124646554-124646660	ENSG00000253286.1
12	lnc-FAM91A1-1	chr8:124628966-124629083	NONHSAT128562

No data

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

Extended variants
information (count: 5617 )
Associated
traits (count: 153 )

Variant overlapped rSNPs/rCNVs (count:5617 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9650084	chr8:124604759-124604760	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs377271298	chr8:124604779-124604780	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs7832861	chr8:124604789-124604790	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs143102195	chr8:124604801-124604802	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150548947	chr8:124604813-124604814	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs75330265	chr8:124604824-124604825	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs570616901	chr8:124604854-124604855	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs527597203	chr8:124604862-124604863	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs78483747	chr8:124604920-124604921	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs146151992	chr8:124604922-124604923	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs535301222	chr8:124604926-124604927	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs139936473	chr8:124605008-124605009	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs149827157	chr8:124605029-124605030	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs543827861	chr8:124605039-124605040	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs557743702	chr8:124605056-124605057	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs578148381	chr8:124605058-124605059	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs540917015	chr8:124605059-124605060	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs537160094	chr8:124605117-124605118	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs71516712	chr8:124605118-124605119	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs145794487	chr8:124605128-124605129	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs115855943	chr8:124605150-124605151	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs181375831	chr8:124605231-124605232	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs373928301	chr8:124605243-124605244	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs185146438	chr8:124605312-124605313	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs531855931	chr8:124605341-124605342	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs189906853	chr8:124605354-124605355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs571615762	chr8:124605355-124605356	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs527727849	chr8:124605409-124605410	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs546859117	chr8:124605427-124605428	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs566459576	chr8:124605430-124605431	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs148434165	chr8:124605439-124605440	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs10104547	chr8:124605447-124605448	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs10089696	chr8:124605525-124605526	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs145105386	chr8:124605567-124605568	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs372189849	chr8:124605589-124605590	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs557614829	chr8:124605613-124605614	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs577555670	chr8:124605620-124605621	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs539881504	chr8:124605625-124605626	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs554481596	chr8:124605695-124605696	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs373842365	chr8:124605746-124605747	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs574405953	chr8:124605771-124605772	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs73705972	chr8:124605788-124605789	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs13265242	chr8:124605830-124605831	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs535253499	chr8:124605849-124605850	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs547344863	chr8:124605863-124605864	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs531861352	chr8:124605866-124605867	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs372650234	chr8:124605938-124605939	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs12547165	chr8:124605960-124605961	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs369694404	chr8:124606013-124606014	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs527665509	chr8:124606030-124606031	Enhancers Weak transcription	Chromatin interactive region	2 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:2353 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124599400-124604800	Enhancers	Stomach Smooth Muscle	stomach
2	chr8:124599400-124605000	Enhancers	Colon Smooth Muscle	Colon
3	chr8:124599600-124606200	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr8:124601200-124605000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr8:124601400-124605400	Enhancers	NHDF-Ad	bronchial
6	chr8:124601400-124607200	Enhancers	Osteobl	bone
7	chr8:124602000-124605400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr8:124602400-124605400	Weak transcription	Right Ventricle	heart
9	chr8:124602400-124609000	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr8:124603200-124604800	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr8:124603400-124604800	Enhancers	Aorta	Aorta
12	chr8:124603400-124604800	Enhancers	Fetal Lung	lung
13	chr8:124603400-124605200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr8:124603400-124605600	Enhancers	NHLF	lung
15	chr8:124603800-124604800	Enhancers	Ovary	ovary
16	chr8:124604000-124605000	Enhancers	Right Atrium	heart
17	chr8:124604000-124605200	Enhancers	NHEK	skin
18	chr8:124604200-124604800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr8:124604200-124605400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr8:124604200-124605600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr8:124604200-124606400	Enhancers	K562	blood
22	chr8:124604200-124606800	Weak transcription	Rectal Smooth Muscle	rectum
23	chr8:124604400-124604800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr8:124604400-124604800	Flanking Active TSS	HMEC	breast
25	chr8:124604400-124605000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr8:124604400-124605000	Enhancers	Psoas Muscle	Psoas
27	chr8:124604400-124605000	Enhancers	HSMM	muscle
28	chr8:124604400-124605200	Enhancers	Muscle Satellite Cultured Cells	--
29	chr8:124604400-124605800	Enhancers	Fetal Stomach	stomach
30	chr8:124604400-124607200	Enhancers	HSMMtube	muscle
31	chr8:124604400-124609200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr8:124604600-124604800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr8:124604600-124604800	Enhancers	Adipose Nuclei	Adipose
34	chr8:124604600-124604800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr8:124604600-124605000	Enhancers	Pancreas	Pancrea
36	chr8:124604800-124605000	Enhancers	HMEC	breast
37	chr8:124604800-124605600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr8:124604800-124605600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr8:124604800-124605600	Weak transcription	Fetal Lung	lung
40	chr8:124604800-124606600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr8:124604800-124607000	Weak transcription	Ovary	ovary
42	chr8:124604800-124607200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr8:124604800-124608600	Weak transcription	Stomach Smooth Muscle	stomach
44	chr8:124604800-124609200	Weak transcription	Aorta	Aorta
45	chr8:124605000-124605400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr8:124605000-124605400	Weak transcription	Psoas Muscle	Psoas
47	chr8:124605000-124605400	Weak transcription	Right Atrium	heart
48	chr8:124605000-124606000	Weak transcription	HMEC	breast
49	chr8:124605000-124606200	Weak transcription	HSMM	muscle
50	chr8:124605000-124608600	Weak transcription	Pancreas	Pancrea

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