Variant report

Variant	nsv886568
Chromosome Location	chr6:119044453-119132164
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1159)
CpG islands
(count:185)
Chromatin interactive
region (count:64)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:119072412-119072526	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:119121678-119121983	K562	blood:	n/a	n/a
3	ARID3A	chr6:119097718-119098102	HepG2	liver:	n/a	n/a
4	ATF1	chr6:119050356-119050452	K562	blood:	n/a	n/a
5	ATF1	chr6:119047094-119047455	K562	blood:	n/a	n/a
6	BACH1	chr6:119082954-119083132	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:119082922-119083174	K562	blood:	n/a	n/a
8	BCLAF1	chr6:119121635-119122077	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:119109918-119110067	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:119047215-119047467	K562	blood:	n/a	n/a
11	BHLHE40	chr6:119061284-119061889	K562	blood:	n/a	n/a
12	BHLHE40	chr6:119121706-119122049	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:119045504-119045682	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:119067355-119067632	K562	blood:	n/a	n/a
15	BHLHE40	chr6:119121689-119122052	K562	blood:	n/a	n/a
16	CBX3	chr6:119121610-119122025	K562	blood:	n/a	n/a
17	CBX3	chr6:119047154-119047466	K562	blood:	n/a	n/a
18	CBX3	chr6:119121660-119121974	K562	blood:	n/a	n/a
19	CBX3	chr6:119117561-119118070	K562	blood:	n/a	n/a
20	CCNT2	chr6:119083015-119083025	K562	blood:	n/a	n/a
21	CCNT2	chr6:119047264-119047268	K562	blood:	n/a	n/a
22	CEBPB	chr6:119092524-119092706	IMR90	lung:	n/a	n/a
23	CEBPB	chr6:119089228-119089406	K562	blood:	n/a	chr6:119089298-119089309
24	CEBPB	chr6:119044964-119045256	HepG2	liver:	n/a	chr6:119045096-119045107
25	CEBPB	chr6:119091768-119091929	HepG2	liver:	n/a	chr6:119091840-119091851
26	CEBPB	chr6:119051762-119051831	HepG2	liver:	n/a	chr6:119051794-119051805 chr6:119051794-119051807
27	CEBPB	chr6:119044934-119045269	K562	blood:	n/a	chr6:119045096-119045107
28	CEBPB	chr6:119089107-119089436	HepG2	liver:	n/a	chr6:119089298-119089309
29	CEBPB	chr6:119105174-119105414	IMR90	lung:	n/a	chr6:119105350-119105363
30	CEBPB	chr6:119090182-119090539	MCF-7	breast:	n/a	chr6:119090384-119090397 chr6:119090415-119090428
31	CEBPB	chr6:119098196-119098477	IMR90	lung:	n/a	n/a
32	CEBPB	chr6:119095853-119095981	HepG2	liver:	n/a	chr6:119095921-119095932
33	CEBPB	chr6:119044916-119045280	K562	blood:	n/a	chr6:119045096-119045107
34	CEBPB	chr6:119090205-119090568	MCF-7	breast:	n/a	chr6:119090384-119090397 chr6:119090415-119090428
35	CEBPB	chr6:119098293-119098433	K562	blood:	n/a	n/a
36	CEBPB	chr6:119044923-119045223	IMR90	lung:	n/a	chr6:119045096-119045107
37	CHD1	chr6:119097468-119098135	IMR90	lung:	n/a	n/a
38	CHD2	chr6:119056593-119056796	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr6:119045572-119045772	GM12878	blood:	n/a	n/a
40	CREB1	chr6:119050307-119050567	GM12878	blood:	n/a	n/a
41	CTCF	chr6:119121731-119121988	Kidney_OC	kidney:	n/a	chr6:119121854-119121863 chr6:119121849-119121865 chr6:119121843-119121864 chr6:119121848-119121866 chr6:119121850-119121863
42	CTCF	chr6:119069840-119069990	AG04449	skin:	n/a	n/a
43	CTCF	chr6:119097776-119098055	Gliobla	brain:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
44	CTCF	chr6:119121723-119121994	LNCaP	prostate:	n/a	chr6:119121854-119121863 chr6:119121849-119121865 chr6:119121843-119121864 chr6:119121848-119121866 chr6:119121850-119121863
45	CTCF	chr6:119056553-119056825	GM12891	blood:	n/a	chr6:119056673-119056691 chr6:119056679-119056688 chr6:119056668-119056689 chr6:119056674-119056690
46	CTCF	chr6:119047300-119047450	GM06990	blood:	n/a	n/a
47	CTCF	chr6:119097800-119097950	BE2_C	brain:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
48	CTCF	chr6:119097755-119098057	K562	blood:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
49	CTCF	chr6:119056640-119056790	SK-N-SH_RA	brain:	n/a	chr6:119056673-119056691 chr6:119056679-119056688 chr6:119056668-119056689 chr6:119056674-119056690
50	CTCF	chr6:119056640-119056790	AG10803	skin:	n/a	chr6:119056673-119056691 chr6:119056679-119056688 chr6:119056668-119056689 chr6:119056674-119056690

(count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:119131733-119131783	NT2-D1	testis:	n/a
2	chr6:119069624-119069674	NT2-D1	testis:	n/a
3	chr6:119131733-119131783	NT2-D1	testis:	n/a
4	chr6:119069624-119069674	NT2-D1	testis:	n/a
5	chr6:119131733-119131783	PANC-1	pancreas:	n/a
6	chr6:119131733-119131783	SK-N-SH_RA	brain:	n/a
7	chr6:119069624-119069674	HRCEpiC	kidney:	n/a
8	chr6:119131733-119131783	HRE	kidney:	n/a
9	chr6:119105122-119105172	AG04449	skin:	fetal
10	chr6:119069624-119069674	AG09319	gingival:	n/a
11	chr6:119069624-119069674	GM12892	blood:	n/a
12	chr6:119105122-119105172	ovcar-3	ovarian:	n/a
13	chr6:119105122-119105172	HRCEpiC	kidney:	n/a
14	chr6:119131733-119131783	HRCEpiC	kidney:	n/a
15	chr6:119105122-119105172	GM12878	blood:	n/a
16	chr6:119105122-119105172	SAEC	small airway:	n/a
17	chr6:119069624-119069674	GM12891	blood:	n/a
18	chr6:119069624-119069674	HAEpiC	amniotic membrane:	n/a
19	chr6:119131733-119131783	SK-N-SH	brain:	n/a
20	chr6:119069624-119069674	H1-hESC	embryonic stem cell:	embryo
21	chr6:119105122-119105172	SK-N-MC	brain:	n/a
22	chr6:119105122-119105172	H1-hESC	embryonic stem cell:	embryo
23	chr6:119069624-119069674	AG04450	lung:	fetal
24	chr6:119105122-119105172	NHBE	bronchial:	n/a
25	chr6:119069624-119069674	AG04449	skin:	fetal
26	chr6:119069624-119069674	HIPEpiC	eye:	n/a
27	chr6:119105122-119105172	GM19239	blood:	n/a
28	chr6:119105122-119105172	HCF	heart:	n/a
29	chr6:119069624-119069674	HMEC	breast:	n/a
30	chr6:119105122-119105172	ProgFib	skin:	n/a
31	chr6:119105122-119105172	SKMC	muscle:	n/a
32	chr6:119131733-119131783	HPAEpiC	pulmonary alveolar:	n/a
33	chr6:119131733-119131783	AG10803	skin:	n/a
34	chr6:119131733-119131783	AG04449	skin:	fetal
35	chr6:119105122-119105172	Caco-2	colon:	n/a
36	chr6:119105122-119105172	AG09309	skin:	n/a
37	chr6:119069624-119069674	MCF-7	breast:	n/a
38	chr6:119131733-119131783	PrEC	prostate:	n/a
39	chr6:119105122-119105172	RPTEC	kidney:	n/a
40	chr6:119131733-119131783	HCM	heart:	n/a
41	chr6:119105122-119105172	A549	lung:	n/a
42	chr6:119131733-119131783	HCF	heart:	n/a
43	chr6:119069624-119069674	CMK	blood:	n/a
44	chr6:119105122-119105172	PFSK-1	brain:	n/a
45	chr6:119069624-119069674	Hepatocyte	liver:	n/a
46	chr6:119069624-119069674	IMR90	lung:	fetal
47	chr6:119131733-119131783	H1-hESC	embryonic stem cell:	embryo
48	chr6:119105122-119105172	HL-60	blood:	n/a
49	chr6:119131733-119131783	HCPEpiC	choroid plexus:	n/a
50	chr6:119069624-119069674	SKMC	muscle:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:118604722..118606041-chr6:119121374..119122599,5	K562	blood:
2	chr6:118939806..118940379-chr6:119121824..119122493,2	MCF-7	breast:
3	chr6:119018340..119019295-chr6:119097391..119098460,8	MCF-7	breast:
4	chr6:119041235..119044070-chr6:119050308..119053179,2	K562	blood:
5	chr6:118970885..118973094-chr6:119064943..119066835,2	MCF-7	breast:
6	chr6:119090089..119093226-chr6:119095000..119099014,4	K562	blood:
7	chr6:119050585..119052961-chr6:119056269..119058945,2	MCF-7	breast:
8	chr6:119066428..119069279-chr6:119071576..119073945,2	K562	blood:
9	chr6:119071895..119074006-chr6:119076150..119078886,2	K562	blood:
10	chr3:10690679..10691531-chr6:119085240..119086216,2	MCF-7	breast:
11	chr6:119091223..119093581-chr6:119115948..119118630,2	MCF-7	breast:
12	chr6:119057902..119060681-chr6:119068005..119070664,2	K562	blood:
13	chr6:119128908..119130462-chr6:119213970..119215913,2	MCF-7	breast:
14	chr6:118971950..118973530-chr6:119120433..119122628,2	K562	blood:
15	chr6:119046985..119049451-chr6:119052347..119054432,2	K562	blood:
16	chr6:119084540..119086156-chr6:119087548..119090160,2	K562	blood:
17	chr6:119066428..119069279-chr6:119071576..119073945,2	K562	blood:
18	chr6:119091223..119093581-chr6:119115948..119118630,2	MCF-7	breast:
19	chr6:119099349..119102563-chr6:119103399..119106439,3	K562	blood:
20	chr6:119095345..119097623-chr6:119099653..119102563,2	K562	blood:
21	chr6:119075050..119077178-chr6:119080430..119083071,2	K562	blood:
22	chr6:119029112..119030655-chr6:119123182..119125902,2	K562	blood:
23	chr6:119049850..119053305-chr6:119053538..119057771,6	K562	blood:
24	chr6:118977602..118979632-chr6:119069204..119070765,2	K562	blood:
25	chr6:119042570..119044815-chr6:119050294..119053179,2	K562	blood:
26	chr6:118604989..118605598-chr6:119097517..119098373,3	K562	blood:
27	chr6:119060047..119062597-chr6:119065156..119068895,3	K562	blood:
28	chr6:119060949..119064802-chr6:119066880..119068506,4	K562	blood:
29	chr6:119125219..119127915-chr6:119131589..119133462,2	MCF-7	breast:
30	chr6:119090089..119093226-chr6:119095000..119099014,4	K562	blood:
31	chr6:119129761..119131785-chr6:119132717..119134280,2	MCF-7	breast:
32	chr6:119026092..119028989-chr6:119074948..119078427,3	K562	blood:
33	chr6:119018692..119019285-chr6:119121454..119122042,2	MCF-7	breast:
34	chr6:119050506..119052588-chr6:119054244..119056935,2	K562	blood:
35	chr6:119057902..119060681-chr6:119068005..119070664,2	K562	blood:
36	chr6:119098916..119101415-chr6:119102887..119105983,3	K562	blood:
37	chr6:119086471..119089736-chr6:119091626..119095598,3	K562	blood:
38	chr6:119125219..119127915-chr6:119131589..119133462,2	MCF-7	breast:
39	chr6:119027726..119029678-chr6:119052215..119053776,2	K562	blood:
40	chr6:119030431..119032047-chr6:119056887..119059760,2	K562	blood:
41	chr6:118886433..118887071-chr6:119121474..119122076,2	MCF-7	breast:
42	chr6:119050506..119052588-chr6:119054244..119056935,2	K562	blood:
43	chr6:119075050..119077178-chr6:119080430..119083071,2	K562	blood:
44	chr6:119060047..119062597-chr6:119065156..119068895,3	K562	blood:
45	chr6:119029029..119031408-chr6:119046060..119049012,2	K562	blood:
46	chr6:119120439..119121965-chr6:119219112..119221592,2	K562	blood:
47	chr6:119029491..119033540-chr6:119042019..119045590,4	K562	blood:
48	chr6:119060949..119064802-chr6:119066880..119068506,4	K562	blood:
49	chr6:119086471..119089736-chr6:119091626..119095598,3	K562	blood:
50	chr6:119084540..119086156-chr6:119087548..119090160,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASF1A-5	chr6:119100386-119100768	NONHSAT114698
2	lnc-ASF1A-5	chr6:119104011-119104294	NONHSAT114700
3	lnc-ASF1A-5	chr6:119103875-119104583	NONHSAT114698
4	lnc-ASF1A-5	chr6:119103871-119104581	NONHSAT114699
5	lnc-ASF1A-5	chr6:119078681-119078767	NONHSAT114698

No data

Variant related genes	Relation type
ENSG00000225549	TF binding region
ENSG00000225549	CpG island
ENSG00000111877	chromatin interactions
ENSG00000225549	chromatin interactions
ENSG00000111860	chromatin interactions
ENSG00000111875	chromatin interactions

Extended variants
information (count: 3248 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:3248 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10499087	chr6:119044453-119044454	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs34257485	chr6:119044468-119044469	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs114934300	chr6:119044471-119044472	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs564418964	chr6:119044476-119044477	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs532003265	chr6:119044536-119044537	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs546731847	chr6:119044539-119044540	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs573386316	chr6:119044562-119044563	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs186281098	chr6:119044582-119044583	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs566717043	chr6:119044611-119044612	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs370385612	chr6:119044654-119044655	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs140462810	chr6:119044685-119044686	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs559033713	chr6:119044701-119044702	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs528143094	chr6:119044730-119044731	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs547977986	chr6:119044747-119044748	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs112237582	chr6:119044812-119044813	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs190699592	chr6:119044841-119044842	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs73515285	chr6:119044842-119044843	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs145625498	chr6:119044887-119044888	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs369486460	chr6:119044912-119044913	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs539854682	chr6:119044956-119044957	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs114147001	chr6:119044971-119044972	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs546814202	chr6:119044990-119044991	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs573258190	chr6:119045038-119045039	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs535990236	chr6:119045073-119045074	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs534953219	chr6:119045084-119045085	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs181310202	chr6:119045138-119045139	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs77210713	chr6:119045185-119045186	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs185333743	chr6:119045276-119045277	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs558806655	chr6:119045281-119045282	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs368981435	chr6:119045315-119045316	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs190584965	chr6:119045358-119045359	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs182721282	chr6:119045412-119045413	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs115689833	chr6:119045439-119045440	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs138501057	chr6:119045446-119045447	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs528066704	chr6:119045462-119045463	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs541941592	chr6:119045491-119045492	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs12661563	chr6:119045545-119045546	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs530754767	chr6:119045591-119045592	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs550760347	chr6:119045612-119045613	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs143052798	chr6:119045629-119045630	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs73515286	chr6:119045630-119045631	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs556911038	chr6:119045651-119045652	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs200045374	chr6:119045720-119045721	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs575265415	chr6:119045766-119045767	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs546911522	chr6:119045767-119045768	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs545881332	chr6:119045882-119045883	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs138966431	chr6:119045950-119045951	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs149396927	chr6:119045954-119045955	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs143961110	chr6:119045967-119045968	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs569221283	chr6:119045984-119045985	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	18698023	CNVD
Mental retardation	18854857	CNVD
Leukemia	18688285	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Liver carcinoma	19366792	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1497 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119031600-119045600	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr6:119039000-119045000	Enhancers	Primary T helper naive cells from peripheral blood	blood
3	chr6:119039000-119045000	Enhancers	Primary T killer memory cells from peripheral blood	blood
4	chr6:119039000-119046000	Enhancers	Primary B cells from peripheral blood	blood
5	chr6:119039400-119048600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
6	chr6:119041000-119045600	Weak transcription	Fetal Lung	lung
7	chr6:119041200-119045600	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr6:119041200-119045600	Weak transcription	K562	blood
9	chr6:119041200-119048200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr6:119042200-119045600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr6:119042200-119046800	Weak transcription	Thymus	Thymus
12	chr6:119042400-119048200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
13	chr6:119043000-119045600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr6:119043000-119046600	Weak transcription	Fetal Thymus	thymus
15	chr6:119043000-119047000	Weak transcription	Dnd41	blood
16	chr6:119043200-119044800	Weak transcription	Primary B cells from cord blood	blood
17	chr6:119043400-119044600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr6:119043600-119044600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr6:119043600-119044600	Enhancers	Osteobl	bone
20	chr6:119043600-119045200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr6:119043800-119044800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr6:119043800-119046600	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr6:119043800-119046800	Weak transcription	Primary T cells from cord blood	blood
24	chr6:119044000-119044800	Enhancers	HMEC	breast
25	chr6:119044000-119044800	Enhancers	NH-A	brain
26	chr6:119044200-119044600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr6:119044200-119044600	Enhancers	Spleen	Spleen
28	chr6:119044200-119044600	Enhancers	NHEK	skin
29	chr6:119044200-119044800	Enhancers	Fetal Muscle Leg	muscle
30	chr6:119044200-119044800	Enhancers	Right Atrium	heart
31	chr6:119044200-119044800	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr6:119044200-119045800	Enhancers	Psoas Muscle	Psoas
33	chr6:119044200-119048400	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr6:119044400-119044800	Enhancers	Left Ventricle	heart
35	chr6:119044400-119045000	Enhancers	Fetal Heart	heart
36	chr6:119044400-119045400	Enhancers	GM12878-XiMat	blood
37	chr6:119044600-119045400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr6:119044600-119045600	Weak transcription	NHEK	skin
39	chr6:119044800-119045600	Enhancers	Primary B cells from cord blood	blood
40	chr6:119045000-119045400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr6:119045000-119045400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr6:119045000-119045400	Weak transcription	Fetal Heart	heart
43	chr6:119045200-119045400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr6:119045200-119045800	Enhancers	Stomach Mucosa	stomach
45	chr6:119045400-119045600	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr6:119045400-119045800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
47	chr6:119045400-119046000	Enhancers	Fetal Heart	heart
48	chr6:119045400-119046000	Flanking Active TSS	GM12878-XiMat	blood
49	chr6:119045400-119047200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr6:119045400-119048400	Enhancers	Primary T killer memory cells from peripheral blood	blood

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Variant report

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