Variant report

Variant	rs12308567
Chromosome Location	chr12:50134388-50134389
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:50134227..50139526-chr12:50218668..50224471,9	K562	blood:
2	chr12:49960831..49963371-chr12:50134082..50136909,3	K562	blood:
3	chr12:50133628..50137162-chr12:50236178..50238766,3	MCF-7	breast:
4	chr12:50099890..50103139-chr12:50133844..50137712,5	MCF-7	breast:
5	chr12:50032692..50036397-chr12:50134121..50137732,4	K562	blood:
6	chr12:50015683..50018623-chr12:50134319..50137008,3	K562	blood:
7	chr12:50015453..50020013-chr12:50133989..50136234,5	MCF-7	breast:
8	chr12:50134183..50135831-chr12:50504154..50505944,2	K562	blood:
9	chr12:49523706..49526236-chr12:50134306..50136655,2	K562	blood:
10	chr12:50097894..50103527-chr12:50133840..50136991,8	K562	blood:
11	chr12:50015484..50017956-chr12:50133972..50136718,3	MCF-7	breast:
12	chr12:50034541..50040504-chr12:50134095..50137099,9	MCF-7	breast:
13	chr12:50133989..50135613-chr12:50163307..50165869,2	K562	blood:
14	chr12:50134100..50136720-chr12:50149997..50152426,2	MCF-7	breast:
15	chr12:49960473..49963349-chr12:50134082..50137265,4	K562	blood:
16	chr12:50133925..50140140-chr12:50217980..50223924,8	K562	blood:
17	chr12:50023902..50034192-chr12:50133489..50138270,11	K562	blood:
18	chr12:50134058..50135690-chr12:50222133..50224042,2	MCF-7	breast:
19	chr12:50134056..50135953-chr20:46129725..46131567,2	MCF-7	breast:
20	chr12:50097260..50102816-chr12:50134110..50137683,7	MCF-7	breast:
21	chr12:50134026..50138215-chr12:50236682..50241219,8	K562	blood:
22	chr12:50096479..50103459-chr12:50133671..50138995,13	K562	blood:

No data

Variant related genes	Relation type
ENSG00000186666	Chromatin interaction
ENSG00000258057	Chromatin interaction
ENSG00000167566	Chromatin interaction
ENSG00000161791	Chromatin interaction
ENSG00000124151	Chromatin interaction
ENSG00000139644	Chromatin interaction
ENSG00000258017	Chromatin interaction
ENSG00000187778	Chromatin interaction
ENSG00000178449	Chromatin interaction
ENSG00000123416	Chromatin interaction
ENSG00000110844	Chromatin interaction
ENSG00000257730	Chromatin interaction
ENSG00000257570	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10160960	0.83[ASN][1000 genomes]
rs10161088	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10219602	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1078216	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11169108	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11169121	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11169128	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11169129	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11169130	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11169132	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11503899	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12304910	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12306114	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12306565	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12309717	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12314676	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12315732	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12321910	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12321935	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28654319	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28755804	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35275181	0.82[ASN][1000 genomes]
rs56784440	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57144906	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58250762	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59511398	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59811112	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60402517	0.85[ASN][1000 genomes]
rs7136772	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7136990	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73306854	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73306885	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73309015	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045327	chr12:49975040-50551375	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	170 gene(s)	inside rSNPs	diseases
2	nsv541490	chr12:49975040-50551375	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	170 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:50128000-50134600	Weak transcription	HepG2	liver
2	chr12:50133400-50134600	Enhancers	Dnd41	blood
3	chr12:50133600-50134600	Weak transcription	K562	blood
4	chr12:50133600-50134800	Weak transcription	HUVEC	blood vessel
5	chr12:50133600-50134800	Weak transcription	NH-A	brain
6	chr12:50134200-50134800	Enhancers	Liver	Liver
7	chr12:50134200-50134800	Enhancers	Fetal Intestine Small	intestine

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