Variant report

Variant	rs8032107
Chromosome Location	chr15:58326834-58326835
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:58324356..58327238-chr15:58338542..58340895,2	K562	blood:
2	chr15:58325674..58328076-chr15:58330159..58331775,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000128918	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10851633	0.86[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs11071365	0.91[ASN][1000 genomes]
rs11071366	0.84[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs11630835	0.87[ASN][1000 genomes]
rs11852540	0.98[ASN][1000 genomes]
rs11855259	0.82[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs11857461	0.96[ASN][1000 genomes]
rs12148093	0.82[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs12148907	0.97[ASN][1000 genomes]
rs12901462	0.97[ASN][1000 genomes]
rs12903474	0.91[ASN][1000 genomes]
rs12903551	0.87[ASN][1000 genomes]
rs12908953	0.95[ASN][1000 genomes]
rs12910113	0.80[ASN][1000 genomes]
rs12910752	0.95[ASN][1000 genomes]
rs12911071	0.95[ASN][1000 genomes]
rs12914590	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12915693	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12915901	0.96[ASN][1000 genomes]
rs1372368	0.84[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs3204689	0.81[ASN][1000 genomes]
rs34871384	0.96[ASN][1000 genomes]
rs35246600	0.84[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs35511675	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs3784260	0.81[ASN][1000 genomes]
rs4369598	0.98[ASN][1000 genomes]
rs4646563	0.80[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs4646568	0.96[ASN][1000 genomes]
rs4646571	0.80[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs4646572	0.92[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs4646576	0.84[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4646586	0.95[ASN][1000 genomes]
rs4646593	0.84[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs4646611	0.88[ASN][1000 genomes]
rs4646612	0.88[ASN][1000 genomes]
rs4646622	0.80[AFR][1000 genomes]
rs4646627	0.84[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs4646628	0.81[ASN][1000 genomes]
rs4646629	0.84[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs4646636	0.81[ASN][1000 genomes]
rs4646638	0.83[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs4646640	0.81[ASN][1000 genomes]
rs7164408	0.81[ASN][1000 genomes]
rs8031133	0.82[ASN][1000 genomes]
rs9325	0.82[AFR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038667	chr15:57933076-58481870	Flanking Active TSS Enhancers Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv542400	chr15:57933076-58481870	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv833023	chr15:58161839-58340174	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv904261	chr15:58258424-58347260	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58325200-58328400	Weak transcription	Fetal Kidney	kidney
2	chr15:58325400-58329200	Weak transcription	K562	blood
3	chr15:58326800-58327200	Enhancers	HMEC	breast
4	chr15:58326800-58327400	Enhancers	NHEK	skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links