Variant report

Variant	rs34704426
Chromosome Location	chr8:124207022-124207023
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:124197444..124199510-chr8:124205893..124207940,2	MCF-7	breast:
2	chr8:124205866..124208638-chr8:124223387..124226315,2	K562	blood:
3	chr8:124202196..124205513-chr8:124205556..124208969,4	K562	blood:
4	chr8:124205722..124208237-chr8:124217531..124219104,2	K562	blood:

Variant related genes	Relation type
ENSG00000253410	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11779458	0.88[EUR][1000 genomes]
rs11779971	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11782844	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11783554	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11786273	0.88[EUR][1000 genomes]
rs13270162	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13271849	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs16898130	0.91[EUR][1000 genomes]
rs17377283	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17377409	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34947160	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35456955	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55724085	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62521846	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62521847	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62521850	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6997530	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6997717	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6997816	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7003842	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs71514800	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7812683	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7813460	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7813708	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7814154	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7814186	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7817153	0.91[EUR][1000 genomes]
rs7817345	0.91[EUR][1000 genomes]
rs7833092	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9693914	0.91[EUR][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	nsv1032827	chr8:123668081-124270400	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv529364	chr8:123763846-124373809	Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv1015249	chr8:124103504-124373949	Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv539741	chr8:124103504-124373949	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124193400-124241200	Weak transcription	Right Atrium	heart
2	chr8:124199800-124216600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr8:124201600-124212600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:124201600-124216000	Strong transcription	NHEK	skin
5	chr8:124201600-124216800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr8:124202800-124211600	Strong transcription	HMEC	breast
7	chr8:124205200-124209000	Strong transcription	K562	blood
8	chr8:124205200-124209200	Weak transcription	Esophagus	oesophagus
9	chr8:124205200-124217600	Weak transcription	Gastric	stomach
10	chr8:124205400-124209200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr8:124206200-124215200	Strong transcription	Hela-S3	cervix
12	chr8:124206600-124207200	Weak transcription	Adipose Nuclei	Adipose

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