Variant report

Variant	rs2488062
Chromosome Location	chr10:94523766-94523767
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:94517024..94521206-chr10:94522377..94524965,5	K562	blood:

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1033976	1.00[ASN][1000 genomes]
rs10466167	1.00[ASN][1000 genomes]
rs10736071	1.00[ASN][1000 genomes]
rs10748586	1.00[ASN][1000 genomes]
rs10786057	1.00[ASN][1000 genomes]
rs1326331	1.00[ASN][1000 genomes]
rs1326332	1.00[ASN][1000 genomes]
rs1409387	1.00[ASN][1000 genomes]
rs2025730	1.00[ASN][1000 genomes]
rs2094232	1.00[ASN][1000 genomes]
rs2148361	1.00[ASN][1000 genomes]
rs2182451	1.00[ASN][1000 genomes]
rs2246370	1.00[ASN][1000 genomes]
rs2246382	1.00[ASN][1000 genomes]
rs2246701	1.00[ASN][1000 genomes]
rs2250393	1.00[ASN][1000 genomes]
rs2422070	1.00[ASN][1000 genomes]
rs2422072	1.00[ASN][1000 genomes]
rs2490732	1.00[ASN][1000 genomes]
rs2490733	1.00[ASN][1000 genomes]
rs2490740	1.00[ASN][1000 genomes]
rs2490742	1.00[ASN][1000 genomes]
rs2490744	1.00[ASN][1000 genomes]
rs2497322	1.00[ASN][1000 genomes]
rs2497323	1.00[ASN][1000 genomes]
rs2497324	1.00[ASN][1000 genomes]
rs2497326	1.00[ASN][1000 genomes]
rs2497327	1.00[ASN][1000 genomes]
rs2497331	1.00[ASN][1000 genomes]
rs2497339	1.00[ASN][1000 genomes]
rs2497347	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2497348	1.00[ASN][1000 genomes]
rs2497350	0.95[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4517429	1.00[ASN][1000 genomes]
rs4933241	1.00[ASN][1000 genomes]
rs4933242	1.00[ASN][1000 genomes]
rs4933749	1.00[ASN][1000 genomes]
rs4933752	1.00[ASN][1000 genomes]
rs6583846	1.00[ASN][1000 genomes]
rs7069070	1.00[ASN][1000 genomes]
rs7070025	1.00[ASN][1000 genomes]
rs7078376	1.00[ASN][1000 genomes]
rs7082382	1.00[ASN][1000 genomes]
rs7089179	1.00[ASN][1000 genomes]
rs7893270	1.00[ASN][1000 genomes]
rs7894145	1.00[ASN][1000 genomes]
rs7909191	1.00[ASN][1000 genomes]
rs7909581	1.00[ASN][1000 genomes]
rs7913340	1.00[ASN][1000 genomes]
rs7914859	1.00[ASN][1000 genomes]
rs9419746	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9420592	0.87[LWK][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs9633695	1.00[ASN][1000 genomes]
rs973733	1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3446249	chr10:94374508-94549394	Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94520800-94525200	Weak transcription	Primary B cells from peripheral blood	blood
2	chr10:94520800-94526000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr10:94522400-94526800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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