Variant report

Variant	nsv10823
Chromosome Location	chr6:31870996-31880226
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:279)
CpG islands
(count:183)
Chromatin interactive
region (count:60)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:279 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:31875170-31875461	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:31876624-31876971	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:31879193-31879474	K562	blood:	n/a	n/a
4	ARID3A	chr6:31878142-31878240	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:31871739-31872027	K562	blood:	n/a	n/a
6	ATF2	chr6:31876511-31877051	GM12878	blood:	n/a	n/a
7	ATF2	chr6:31876453-31877059	GM12878	blood:	n/a	n/a
8	ATF3	chr6:31879212-31879447	K562	blood:	n/a	n/a
9	ATF3	chr6:31879116-31879438	K562	blood:	n/a	n/a
10	BATF	chr6:31879152-31879398	GM12878	blood:	n/a	chr6:31879356-31879367 chr6:31879331-31879342
11	BATF	chr6:31879156-31879480	GM12878	blood:	n/a	chr6:31879356-31879367 chr6:31879331-31879342
12	BATF	chr6:31876490-31876927	GM12878	blood:	n/a	n/a
13	BATF	chr6:31876477-31876959	GM12878	blood:	n/a	n/a
14	BCL11A	chr6:31876589-31876925	GM12878	blood:	n/a	n/a
15	BCL11A	chr6:31879171-31879493	GM12878	blood:	n/a	n/a
16	BCL3	chr6:31876527-31876931	GM12878	blood:	n/a	n/a
17	BCLAF1	chr6:31876542-31876935	GM12878	blood:	n/a	n/a
18	BCLAF1	chr6:31876612-31877015	GM12878	blood:	n/a	n/a
19	BHLHE40	chr6:31875228-31875331	HepG2	liver:	n/a	n/a
20	BHLHE40	chr6:31876632-31876960	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:31871776-31872018	K562	blood:	n/a	n/a
22	CBX3	chr6:31877890-31878576	HCT-116	colon:	n/a	n/a
23	CBX3	chr6:31879153-31879556	HCT-116	colon:	n/a	n/a
24	CEBPB	chr6:31875130-31875502	A549	lung:	n/a	chr6:31875339-31875350
25	CEBPB	chr6:31875155-31875513	H1-hESC	embryonic stem cell:	n/a	chr6:31875339-31875350
26	CEBPB	chr6:31875093-31875551	HepG2	liver:	n/a	chr6:31875339-31875350
27	CEBPB	chr6:31878443-31878571	IMR90	lung:	n/a	n/a
28	CEBPB	chr6:31875133-31875532	Hela-S3	cervix:	n/a	chr6:31875339-31875350
29	CEBPB	chr6:31875147-31875520	HepG2	liver:	n/a	chr6:31875339-31875350
30	CEBPB	chr6:31875114-31875485	MCF-7	breast:	n/a	chr6:31875339-31875350
31	CEBPB	chr6:31875201-31875473	ECC-1	luminal epithelium:	n/a	chr6:31875339-31875350
32	CEBPB	chr6:31875144-31875494	HepG2	liver:	n/a	chr6:31875339-31875350
33	CEBPB	chr6:31875140-31875483	A549	lung:	n/a	chr6:31875339-31875350
34	CEBPB	chr6:31875091-31875488	MCF-7	breast:	n/a	chr6:31875339-31875350
35	CEBPB	chr6:31875145-31875527	HepG2	liver:	n/a	chr6:31875339-31875350
36	CEBPB	chr6:31876347-31876816	IMR90	lung:	n/a	n/a
37	CEBPB	chr6:31875146-31875524	IMR90	lung:	n/a	chr6:31875339-31875350
38	CEBPB	chr6:31875110-31875482	ECC-1	luminal epithelium:	n/a	chr6:31875339-31875350
39	CEBPB	chr6:31879065-31879499	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr6:31875154-31875523	A549	lung:	n/a	chr6:31875339-31875350
41	CEBPB	chr6:31879032-31879457	IMR90	lung:	n/a	n/a
42	CEBPB	chr6:31875187-31875454	K562	blood:	n/a	chr6:31875339-31875350
43	CEBPB	chr6:31875146-31875536	K562	blood:	n/a	chr6:31875339-31875350
44	CEBPB	chr6:31875071-31875545	K562	blood:	n/a	chr6:31875339-31875350
45	CEBPD	chr6:31875071-31875451	HepG2	liver:	n/a	n/a
46	CEBPD	chr6:31875088-31875512	K562	blood:	n/a	n/a
47	CEBPD	chr6:31875105-31875424	HepG2	liver:	n/a	n/a
48	CTCF	chr6:31878800-31878950	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr6:31878984-31879034	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:31878974-31879048	MCF-7	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31870990-31871040	HNPCEpiC	eye:	n/a
2	chr6:31873772-31873822	GM12892	blood:	n/a
3	chr6:31870990-31871040	GM06990	blood:	n/a
4	chr6:31873772-31873822	HIPEpiC	eye:	n/a
5	chr6:31873772-31873822	HepG2	liver:	n/a
6	chr6:31870990-31871040	MCF-7	breast:	n/a
7	chr6:31870970-31871020	SK-N-SH_RA	brain:	n/a
8	chr6:31873772-31873822	GM12878	blood:	n/a
9	chr6:31870970-31871020	Caco-2	colon:	n/a
10	chr6:31870990-31871040	SK-N-SH	brain:	n/a
11	chr6:31873772-31873822	PFSK-1	brain:	n/a
12	chr6:31870990-31871040	Caco-2	colon:	n/a
13	chr6:31873772-31873822	BJ	skin:	n/a
14	chr6:31870970-31871020	AG04449	skin:	fetal
15	chr6:31873772-31873822	HAEpiC	amniotic membrane:	n/a
16	chr6:31870970-31871020	HEEpiC	esophagus:	n/a
17	chr6:31873772-31873822	HCM	heart:	n/a
18	chr6:31870990-31871040	HRE	kidney:	n/a
19	chr6:31873772-31873822	HEEpiC	esophagus:	n/a
20	chr6:31870990-31871040	HMEC	breast:	n/a
21	chr6:31873772-31873822	PrEC	prostate:	n/a
22	chr6:31870990-31871040	HPAEpiC	pulmonary alveolar:	n/a
23	chr6:31873772-31873822	SK-N-SH_RA	brain:	n/a
24	chr6:31870990-31871040	H1-hESC	embryonic stem cell:	embryo
25	chr6:31870990-31871040	NB4	blood:	n/a
26	chr6:31870990-31871040	HUVEC	blood vessel:	n/a
27	chr6:31870990-31871040	HepG2	liver:	n/a
28	chr6:31870970-31871020	A549	lung:	n/a
29	chr6:31870990-31871040	A549	lung:	n/a
30	chr6:31870990-31871040	IMR90	lung:	fetal
31	chr6:31870990-31871040	GM12892	blood:	n/a
32	chr6:31870990-31871040	Jurkat	blood:	n/a
33	chr6:31870970-31871020	NHBE	bronchial:	n/a
34	chr6:31870990-31871040	SAEC	small airway:	n/a
35	chr6:31870970-31871020	GM12878	blood:	n/a
36	chr6:31870970-31871020	HCF	heart:	n/a
37	chr6:31873772-31873822	SK-N-MC	brain:	n/a
38	chr6:31870970-31871020	Jurkat	blood:	n/a
39	chr6:31870970-31871020	PANC-1	pancreas:	n/a
40	chr6:31870970-31871020	BE2_C	brain:	n/a
41	chr6:31870970-31871020	SK-N-SH	brain:	n/a
42	chr6:31870990-31871040	K562	blood:	n/a
43	chr6:31873772-31873822	AoSMC	blood vessel:	n/a
44	chr6:31870990-31871040	HCF	heart:	n/a
45	chr6:31873772-31873822	SAEC	small airway:	n/a
46	chr6:31870970-31871020	AG09309	skin:	n/a
47	chr6:31873772-31873822	HUVEC	blood vessel:	n/a
48	chr6:31870990-31871040	PANC-1	pancreas:	n/a
49	chr6:31870970-31871020	HMEC	breast:	n/a
50	chr6:31870970-31871020	Hela-S3	cervix:	n/a

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:31871171..31873867-chr6:31879950..31882707,2	K562	blood:
2	chr6:31866210..31871385-chr6:31935988..31941288,8	K562	blood:
3	chr6:31868781..31871119-chr6:31892943..31895660,2	MCF-7	breast:
4	chr6:31878620..31883206-chr6:31886639..31889995,5	K562	blood:
5	chr6:31864641..31866622-chr6:31876765..31878886,2	K562	blood:
6	chr6:31878808..31881745-chr6:31887583..31889683,2	MCF-7	breast:
7	chr17:61904476..61906775-chr6:31869076..31871321,2	MCF-7	breast:
8	chr6:31864741..31867831-chr6:31872315..31875298,3	K562	blood:
9	chr6:31742944..31744994-chr6:31869511..31871431,2	K562	blood:
10	chr6:31508952..31511301-chr6:31870064..31872291,2	MCF-7	breast:
11	chr6:31869231..31871840-chr6:31901304..31905157,3	MCF-7	breast:
12	chr6:31874923..31879806-chr6:31881504..31885897,6	K562	blood:
13	chr6:31870200..31872258-chr6:31872448..31875801,4	K562	blood:
14	chr6:31631113..31634365-chr6:31867924..31871902,6	K562	blood:
15	chr6:31869703..31871388-chr6:31919073..31921188,2	K562	blood:
16	chr6:31509091..31511742-chr6:31868193..31871571,3	MCF-7	breast:
17	chr6:31870972..31872047-chr6:31920053..31920679,3	MCF-7	breast:
18	chr6:31876714..31878238-chr6:31917519..31919681,2	MCF-7	breast:
19	chr6:31868360..31871056-chr6:32011358..32014091,3	K562	blood:
20	chr6:31870200..31872258-chr6:31872448..31875801,4	K562	blood:
21	chr6:31829040..31831339-chr6:31870895..31873682,3	K562	blood:
22	chr6:31868564..31871785-chr6:31887319..31890291,4	MCF-7	breast:
23	chr6:31869193..31873526-chr6:31908186..31911581,4	MCF-7	breast:
24	chr6:31875081..31878398-chr6:31887360..31892361,5	MCF-7	breast:
25	chr17:56735218..56737822-chr6:31869690..31871981,3	MCF-7	breast:
26	chr6:31867614..31871926-chr6:31937988..31942087,9	K562	blood:
27	chr6:31801352..31804698-chr6:31868339..31871951,3	K562	blood:
28	chr6:31871344..31873109-chr6:31927520..31930389,2	K562	blood:
29	chr6:31867895..31873109-chr6:31925613..31930389,7	K562	blood:
30	chr6:31831382..31834219-chr6:31869960..31872088,3	K562	blood:
31	chr6:31794734..31796775-chr6:31868219..31871084,2	MCF-7	breast:
32	chr6:31868706..31872478-chr6:31938286..31942065,5	MCF-7	breast:
33	chr6:31878159..31881890-chr6:31886214..31889355,6	MCF-7	breast:
34	chr6:31586050..31587690-chr6:31877612..31880010,2	K562	blood:
35	chr6:31841453..31844170-chr6:31871431..31873246,2	MCF-7	breast:
36	chr6:31866937..31870954-chr6:31878649..31881648,4	K562	blood:
37	chr6:31870028..31871569-chr6:31882046..31884323,2	K562	blood:
38	chr6:31863769..31866724-chr6:31879168..31880795,3	K562	blood:
39	chr6:31867879..31871842-chr6:31901664..31905567,4	MCF-7	breast:
40	chr6:31630438..31633368-chr6:31873885..31875945,2	K562	blood:
41	chr6:31627970..31635325-chr6:31864036..31871429,12	K562	blood:
42	chr6:31870410..31872012-chr6:32054069..32057423,3	K562	blood:
43	chr6:31873514..31876453-chr6:31939524..31941298,2	K562	blood:
44	chr6:31864068..31872693-chr6:31934470..31941847,12	MCF-7	breast:
45	chr6:31862879..31872535-chr6:31911667..31928766,47	MCF-7	breast:
46	chr6:31812130..31814477-chr6:31875072..31877975,2	K562	blood:
47	chr6:31864040..31872511-chr6:31917614..31930102,27	MCF-7	breast:
48	chr6:31873769..31875382-chr6:31938198..31940926,2	MCF-7	breast:
49	chr6:31829023..31831554-chr6:31869870..31871779,2	MCF-7	breast:
50	chr6:31761659..31764051-chr6:31869423..31871582,3	K562	blood:

No data

Variant related genes	Relation type
ZBTB12	TF binding region
ZBTB12	CpG island
ENSG00000204366	chromatin interactions
ENSG00000204351	chromatin interactions
ENSG00000087191	chromatin interactions
ENSG00000204385	chromatin interactions
ENSG00000221267	chromatin interactions
ENSG00000234006	chromatin interactions
ENSG00000244255	chromatin interactions
ENSG00000265236	chromatin interactions
ENSG00000168477	chromatin interactions
ENSG00000204396	chromatin interactions
ENSG00000204439	chromatin interactions
ENSG00000201207	chromatin interactions
ENSG00000204438	chromatin interactions
ENSG00000108592	chromatin interactions
ENSG00000243649	chromatin interactions
ENSG00000204348	chromatin interactions
ENSG00000204344	chromatin interactions
ENSG00000204394	chromatin interactions
ENSG00000204386	chromatin interactions
ENSG00000201823	chromatin interactions
ENSG00000213722	chromatin interactions
ENSG00000201754	chromatin interactions
ENSG00000204387	chromatin interactions
ENSG00000204371	chromatin interactions
ENSG00000166278	chromatin interactions
ENSG00000263020	chromatin interactions
ENSG00000198563	chromatin interactions
ENSG00000204388	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000204356	chromatin interactions
ENSG00000204435	chromatin interactions

Extended variants
information (count: 236 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:236 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9267666	chr6:31870998-31870999	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
2	rs537842570	chr6:31871052-31871053	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
3	rs537766884	chr6:31871097-31871098	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	27 gene(s)	Overlapped CNVs	n/a
4	rs368933099	chr6:31871117-31871118	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	27 gene(s)	Overlapped CNVs	n/a
5	rs62395849	chr6:31871125-31871126	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	26 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs189206497	chr6:31871127-31871128	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
7	rs372645172	chr6:31871144-31871145	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
8	rs9469071	chr6:31871163-31871164	Weak transcription Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
9	rs559876148	chr6:31871170-31871171	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
10	rs572014752	chr6:31871172-31871173	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
11	rs112525061	chr6:31871204-31871205	Weak transcription Enhancers	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
12	rs140128047	chr6:31871224-31871225	Weak transcription Enhancers	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
13	rs193268593	chr6:31871268-31871269	Weak transcription Enhancers	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
14	rs143928576	chr6:31871281-31871282	Weak transcription Enhancers	Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
15	rs572129543	chr6:31871330-31871331	Weak transcription Enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
16	rs542227007	chr6:31871383-31871384	Weak transcription Enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
17	rs146389066	chr6:31871486-31871487	Weak transcription Enhancers	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
18	rs575910797	chr6:31871559-31871560	Weak transcription Enhancers	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
19	rs561019113	chr6:31871564-31871565	Weak transcription Enhancers	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
20	rs148576683	chr6:31871639-31871640	Weak transcription Enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
21	rs369449420	chr6:31871664-31871665	Weak transcription Enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
22	rs552883443	chr6:31871727-31871728	Weak transcription Enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
23	rs11755921	chr6:31871754-31871755	Weak transcription Enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
24	rs564729464	chr6:31871821-31871822	Weak transcription Enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
25	rs532134132	chr6:31872050-31872051	Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
26	rs184138185	chr6:31872089-31872090	Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
27	rs570334519	chr6:31872104-31872105	Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
28	rs559552853	chr6:31872121-31872122	Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
29	rs530246624	chr6:31872190-31872191	Weak transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
30	rs548266461	chr6:31872213-31872214	Weak transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
31	rs200511047	chr6:31872257-31872258	Weak transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
32	rs142720403	chr6:31872258-31872259	Weak transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
33	rs570110363	chr6:31872280-31872281	Weak transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
34	rs189464203	chr6:31872313-31872314	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs552860655	chr6:31872324-31872325	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs10947223	chr6:31872383-31872384	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs532209523	chr6:31872399-31872400	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs151132610	chr6:31872421-31872422	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs140237193	chr6:31872464-31872465	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs531342527	chr6:31872515-31872516	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs118146343	chr6:31872523-31872524	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs554142968	chr6:31872539-31872540	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs375642552	chr6:31872561-31872562	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs534127670	chr6:31872594-31872595	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs181053016	chr6:31872662-31872663	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs533787393	chr6:31872691-31872692	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs374395291	chr6:31872706-31872707	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs540852145	chr6:31872726-31872727	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs145127917	chr6:31872766-31872767	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs147623247	chr6:31872787-31872788	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:131)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ovarian cancer	21781307	CNVD
Ependymoma	19289631	CNVD
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Breast cancer	21364760	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	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
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:247 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31870000-31871000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr6:31870000-31871000	Flanking Active TSS	Dnd41	blood
3	chr6:31870200-31871000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr6:31870200-31871000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr6:31870200-31871000	Flanking Active TSS	Adipose Nuclei	Adipose
6	chr6:31870200-31871000	Flanking Active TSS	Duodenum Mucosa	Duodenum
7	chr6:31870200-31871000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
8	chr6:31870200-31871000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
9	chr6:31870200-31871000	Flanking Active TSS	Stomach Smooth Muscle	stomach
10	chr6:31870400-31871000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr6:31870400-31871000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:31870400-31871000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr6:31870400-31871000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
14	chr6:31870400-31871000	Flanking Active TSS	Colon Smooth Muscle	Colon
15	chr6:31870400-31871000	Flanking Active TSS	Fetal Intestine Large	intestine
16	chr6:31870400-31871000	Flanking Active TSS	Fetal Intestine Small	intestine
17	chr6:31870400-31871000	Flanking Active TSS	Fetal Kidney	kidney
18	chr6:31870400-31871000	Flanking Active TSS	Pancreas	Pancrea
19	chr6:31870400-31871000	Enhancers	Spleen	Spleen
20	chr6:31870400-31871000	Flanking Active TSS	HepG2	liver
21	chr6:31870400-31871000	Flanking Active TSS	NHDF-Ad	bronchial
22	chr6:31870600-31871000	Enhancers	H9 Cell Line	embryonic stem cell
23	chr6:31870600-31871000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr6:31870600-31871000	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr6:31870600-31871000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr6:31870600-31871000	Enhancers	Primary B cells from cord blood	blood
27	chr6:31870600-31871000	Enhancers	Primary B cells from peripheral blood	blood
28	chr6:31870600-31871000	Enhancers	Primary T cells fromperipheralblood	blood
29	chr6:31870600-31871000	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr6:31870600-31871000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr6:31870600-31871000	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr6:31870600-31871000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr6:31870600-31871000	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr6:31870600-31871000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr6:31870600-31871000	Enhancers	Brain Angular Gyrus	brain
36	chr6:31870600-31871000	Enhancers	Esophagus	oesophagus
37	chr6:31870600-31871000	Enhancers	Fetal Brain Female	brain
38	chr6:31870600-31871000	Enhancers	Gastric	stomach
39	chr6:31870600-31871000	Enhancers	Left Ventricle	heart
40	chr6:31870600-31871000	Enhancers	Lung	lung
41	chr6:31870600-31871000	Flanking Active TSS	Rectal Smooth Muscle	rectum
42	chr6:31870600-31871000	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr6:31870600-31871000	Enhancers	Stomach Mucosa	stomach
44	chr6:31870600-31871200	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr6:31870600-31871200	Enhancers	Fetal Heart	heart
46	chr6:31870600-31871200	Enhancers	Fetal Thymus	thymus
47	chr6:31870600-31871400	Enhancers	Liver	Liver
48	chr6:31870600-31873600	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr6:31870600-31873600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr6:31870600-31873600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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