Variant report

Variant	rs6885341
Chromosome Location	chr5:90565796-90565797
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:90555805..90566288-chr5:90673548..90682139,22	K562	blood:
2	chr5:90560937..90569122-chr5:90675177..90680484,12	K562	blood:

Variant related genes	Relation type
ENSG00000113369	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10038090	0.93[ASN][1000 genomes]
rs10061355	0.95[ASN][1000 genomes]
rs10462343	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10462492	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10474346	0.97[ASN][1000 genomes]
rs10474347	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12697807	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13171635	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1511344	0.88[ASN][1000 genomes]
rs1511345	0.80[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1543066	0.93[ASN][1000 genomes]
rs1858309	0.93[ASN][1000 genomes]
rs2048451	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2048452	1.00[ASN][1000 genomes]
rs2973441	0.92[ASN][1000 genomes]
rs4019243	0.88[ASN][1000 genomes]
rs4019302	0.93[ASN][1000 genomes]
rs4364415	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4377733	0.96[ASN][1000 genomes]
rs4424024	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4518439	0.90[ASN][1000 genomes]
rs6859170	0.94[ASN][1000 genomes]
rs6869552	0.91[ASN][1000 genomes]
rs6882172	0.94[ASN][1000 genomes]
rs6888389	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6888674	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6889197	1.00[ASN][1000 genomes]
rs6897578	0.94[ASN][1000 genomes]
rs6898622	0.90[ASN][1000 genomes]
rs7709572	0.94[ASN][1000 genomes]
rs7719516	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7724489	0.94[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	nsv1024813	chr5:90321535-90870739	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
2	nsv537806	chr5:90321535-90870739	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:90562600-90573200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr5:90562800-90568000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr5:90562800-90568600	Weak transcription	Hela-S3	cervix
4	chr5:90562800-90568800	Weak transcription	Fetal Heart	heart
5	chr5:90564200-90566000	Enhancers	Fetal Thymus	thymus
6	chr5:90564400-90566200	Enhancers	Thymus	Thymus
7	chr5:90564600-90565800	Enhancers	Primary T cells from cord blood	blood
8	chr5:90564600-90566200	Enhancers	Dnd41	blood
9	chr5:90564800-90566000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr5:90565000-90575200	Weak transcription	Brain Anterior Caudate	brain
11	chr5:90565200-90566200	Weak transcription	K562	blood
12	chr5:90565600-90568000	Weak transcription	GM12878-XiMat	blood
13	chr5:90565600-90568600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr5:90565600-90568600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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